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6505-01-108-9617

20 Products

NDC00094-0040-06

DOPAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505011089617

NSN

6505-01-108-9617

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NDC00094-0040-06

DOPAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505011089617

NSN

6505-01-108-9617

MFG

DU PONT CRITICAL CARE INC SUB OF E I DU PONT DE NEMOURS AND CO INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS DOPAMINE HYDROCHLORIDE PER CUBIC CENTIMETER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL

NDC00074-5820-01

DOPAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505011089617

NSN

6505-01-108-9617

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NDC00074-5820-01

DOPAMINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505011089617

NSN

6505-01-108-9617

MFG

ABBOTT LABORATORIES INC. DIV HOSPITAL PRODUCTS DIVISION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS DOPAMINE HYDROCHLORIDE PER CUBIC CENTIMETER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL

NDC00024-1353-01

PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION,USP

NSN, MFG P/N

6505011094221

NSN

6505-01-109-4221

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NDC00024-1353-01

PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION,USP

NSN, MFG P/N

6505011094221

NSN

6505-01-109-4221

MFG

SANOFI-SYNTHELABO INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 PERCENTAGE, W/V PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION USP 15ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 15.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC SQUEEZE

NEO-SYNEPHRINE

PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION,USP

NSN, MFG P/N

6505011094221

NSN

6505-01-109-4221

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NEO-SYNEPHRINE

PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION,USP

NSN, MFG P/N

6505011094221

NSN

6505-01-109-4221

MFG

SANOFI-SYNTHELABO INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 PERCENTAGE, W/V PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION USP 15ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 15.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC SQUEEZE

NEO-SYNEPHRINE SPRAY

PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION,USP

NSN, MFG P/N

6505011094221

NSN

6505-01-109-4221

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NEO-SYNEPHRINE SPRAY

PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION,USP

NSN, MFG P/N

6505011094221

NSN

6505-01-109-4221

MFG

SANOFI-SYNTHELABO INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 PERCENTAGE, W/V PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYLEPHRINE HYDROCHLORIDE NASAL SOLUTION USP 15ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 15.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC SQUEEZE

C71

MULTIVITAMIN TABLETS

NSN, MFG P/N

6505011098165

NSN

6505-01-109-8165

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C71

MULTIVITAMIN TABLETS

NSN, MFG P/N

6505011098165

NSN

6505-01-109-8165

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 75.000 MILLIGRAMS ASCORBIC ACID ACTIVE INGREDIENT AND 3.000 MICROGRAMS CYANOCOBALAMIN ACTIVE INGREDIENT AND 25.000 MILLIGRAMS NIACINAMIDE ACTIVE INGREDIENT AND 5.000 MILLIGRAMS PANTOTHENIC ACID ACTIVE INGREDIENT AND 1.200 MILLIGRAMS PYRIDOXINE ACTIVE
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 TABLETS
PRIMARY CONTAINER TYPE: STRIP
SPECIAL FEATURES: 100 INDIVIDUALLY SEALED TABLETS;COATING FEATURE:SUGAR;ADMINISTRATION:ORAL NONCHEWABLE;
TOTAL PRIMARY CONTAINER QUANTITY: 10
~1: INGREDIENT AND 3.000 MILLIGRAMS RIBOFLAVIN ACTIVE INGREDIENT AND 3.000 MILLIGRAMS THIAMINE ACTIVE INGREDIENT AND 10000.000 INTERNATIONAL UNITS VITAMIN A ACTIVE INGREDIENT AND 400.000 INTERNATIONAL UNITS VITAMIN D ACTIVE INGREDIENT AND 6.600 INTERNATIONAL
~2: UNITS VITAMIN E ACTIVE INGREDIENT

MULTICEBRIN

MULTIVITAMIN TABLETS

NSN, MFG P/N

6505011098165

NSN

6505-01-109-8165

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MULTICEBRIN

MULTIVITAMIN TABLETS

NSN, MFG P/N

6505011098165

NSN

6505-01-109-8165

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 75.000 MILLIGRAMS ASCORBIC ACID ACTIVE INGREDIENT AND 3.000 MICROGRAMS CYANOCOBALAMIN ACTIVE INGREDIENT AND 25.000 MILLIGRAMS NIACINAMIDE ACTIVE INGREDIENT AND 5.000 MILLIGRAMS PANTOTHENIC ACID ACTIVE INGREDIENT AND 1.200 MILLIGRAMS PYRIDOXINE ACTIVE
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 TABLETS
PRIMARY CONTAINER TYPE: STRIP
SPECIAL FEATURES: 100 INDIVIDUALLY SEALED TABLETS;COATING FEATURE:SUGAR;ADMINISTRATION:ORAL NONCHEWABLE;
TOTAL PRIMARY CONTAINER QUANTITY: 10
~1: INGREDIENT AND 3.000 MILLIGRAMS RIBOFLAVIN ACTIVE INGREDIENT AND 3.000 MILLIGRAMS THIAMINE ACTIVE INGREDIENT AND 10000.000 INTERNATIONAL UNITS VITAMIN A ACTIVE INGREDIENT AND 400.000 INTERNATIONAL UNITS VITAMIN D ACTIVE INGREDIENT AND 6.600 INTERNATIONAL
~2: UNITS VITAMIN E ACTIVE INGREDIENT

NDC00002-0371-33

MULTIVITAMIN TABLETS

NSN, MFG P/N

6505011098165

NSN

6505-01-109-8165

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NDC00002-0371-33

MULTIVITAMIN TABLETS

NSN, MFG P/N

6505011098165

NSN

6505-01-109-8165

MFG

ELI LILLY AND COMPANY DBA ELI LILLY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 75.000 MILLIGRAMS ASCORBIC ACID ACTIVE INGREDIENT AND 3.000 MICROGRAMS CYANOCOBALAMIN ACTIVE INGREDIENT AND 25.000 MILLIGRAMS NIACINAMIDE ACTIVE INGREDIENT AND 5.000 MILLIGRAMS PANTOTHENIC ACID ACTIVE INGREDIENT AND 1.200 MILLIGRAMS PYRIDOXINE ACTIVE
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 TABLETS
PRIMARY CONTAINER TYPE: STRIP
SPECIAL FEATURES: 100 INDIVIDUALLY SEALED TABLETS;COATING FEATURE:SUGAR;ADMINISTRATION:ORAL NONCHEWABLE;
TOTAL PRIMARY CONTAINER QUANTITY: 10
~1: INGREDIENT AND 3.000 MILLIGRAMS RIBOFLAVIN ACTIVE INGREDIENT AND 3.000 MILLIGRAMS THIAMINE ACTIVE INGREDIENT AND 10000.000 INTERNATIONAL UNITS VITAMIN A ACTIVE INGREDIENT AND 400.000 INTERNATIONAL UNITS VITAMIN D ACTIVE INGREDIENT AND 6.600 INTERNATIONAL
~2: UNITS VITAMIN E ACTIVE INGREDIENT

NDC00597-0017-90

DIPYRIDAMOLE TABLETS,USP

NSN, MFG P/N

6505011099469

NSN

6505-01-109-9469

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NDC00597-0017-90

DIPYRIDAMOLE TABLETS,USP

NSN, MFG P/N

6505011099469

NSN

6505-01-109-9469

MFG

BOEHRINGER INGELHEIM PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 25.000 MILLIGRAMS DIPYRIDAMOLE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,BOEHRINGER-INGLEHEIM

PERSANTINE

DIPYRIDAMOLE TABLETS,USP

NSN, MFG P/N

6505011099469

NSN

6505-01-109-9469

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PERSANTINE

DIPYRIDAMOLE TABLETS,USP

NSN, MFG P/N

6505011099469

NSN

6505-01-109-9469

MFG

BOEHRINGER INGELHEIM PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 25.000 MILLIGRAMS DIPYRIDAMOLE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 90.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,BOEHRINGER-INGLEHEIM

NDC00703-3524-01

DEXAMETHASONE SODIUM PHOSPHATE INJECTION,USP

NSN, MFG P/N

6505011099472

NSN

6505-01-109-9472

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NDC00703-3524-01

DEXAMETHASONE SODIUM PHOSPHATE INJECTION,USP

NSN, MFG P/N

6505011099472

NSN

6505-01-109-9472

MFG

SICOR PHARMACEUTICALS SALES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS DEXAMETHASONE SODIUM PHOSPHATE PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEXAMETHASONE SODIUM PHOSPHATE INJECTION USP 10MG/ML 10ML VIAL
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,ORGANON
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

CORGARD TABLETS

NADOLOL TABLETS,USP

NSN, MFG P/N

6505011101994

NSN

6505-01-110-1994

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CORGARD TABLETS

NADOLOL TABLETS,USP

NSN, MFG P/N

6505011101994

NSN

6505-01-110-1994

MFG

SQUIBB E R AND SONS INC WORLD HQ

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 80.000 MILLIGRAMS NADOLOL ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: NADOLOL TABLETS USP 80MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00003-0241-76

NADOLOL TABLETS,USP

NSN, MFG P/N

6505011101994

NSN

6505-01-110-1994

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NDC00003-0241-76

NADOLOL TABLETS,USP

NSN, MFG P/N

6505011101994

NSN

6505-01-110-1994

MFG

KING PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 80.000 MILLIGRAMS NADOLOL ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: NADOLOL TABLETS USP 80MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00378-1132-01

NADOLOL TABLETS,USP

NSN, MFG P/N

6505011101994

NSN

6505-01-110-1994

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NDC00378-1132-01

NADOLOL TABLETS,USP

NSN, MFG P/N

6505011101994

NSN

6505-01-110-1994

MFG

MYLAN PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 80.000 MILLIGRAMS NADOLOL ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: NADOLOL TABLETS USP 80MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

DILANTIN

PHENYTOIN TABLETS,USP

NSN, MFG P/N

6505011102026

NSN

6505-01-110-2026

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DILANTIN

PHENYTOIN TABLETS,USP

NSN, MFG P/N

6505011102026

NSN

6505-01-110-2026

MFG

PARKE-DAVIS DIV OF WARNER-LAMBERT CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS PHENYTOIN ACTIVE INGREDIENT
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYTOIN TABLETS USP 50MG 100S PG
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 TABLETS
PRIMARY CONTAINER TYPE: PACKAGE
SPECIAL FEATURES: MEDSEP ITEM FOR DOD,PARKE-DAVIS
TOTAL PRIMARY CONTAINER QUANTITY: 10

DILANTIN INFATABS

PHENYTOIN TABLETS,USP

NSN, MFG P/N

6505011102026

NSN

6505-01-110-2026

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DILANTIN INFATABS

PHENYTOIN TABLETS,USP

NSN, MFG P/N

6505011102026

NSN

6505-01-110-2026

MFG

PARKE-DAVIS DIV OF WARNER-LAMBERT CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS PHENYTOIN ACTIVE INGREDIENT
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYTOIN TABLETS USP 50MG 100S PG
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 TABLETS
PRIMARY CONTAINER TYPE: PACKAGE
SPECIAL FEATURES: MEDSEP ITEM FOR DOD,PARKE-DAVIS
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00071-0007-40

PHENYTOIN TABLETS,USP

NSN, MFG P/N

6505011102026

NSN

6505-01-110-2026

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NDC00071-0007-40

PHENYTOIN TABLETS,USP

NSN, MFG P/N

6505011102026

NSN

6505-01-110-2026

MFG

PFIZER INC. DBA PFIZER

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS PHENYTOIN ACTIVE INGREDIENT
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYTOIN TABLETS USP 50MG 100S PG
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 TABLETS
PRIMARY CONTAINER TYPE: PACKAGE
SPECIAL FEATURES: MEDSEP ITEM FOR DOD,PARKE-DAVIS
TOTAL PRIMARY CONTAINER QUANTITY: 10

0201

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

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0201

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

MFG

CETYLITE INDUSTRIES INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 PERCENTAGE, W/V BENZALKONIUM CHLORIDE ACTIVE INGREDIENT AND 14.000 PERCENTAGE, W/V BENZOCAINE ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V BUTAMBEN ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V TETRACAINE HYDROCHLORIDE ACTIVE INGREDIENT AND 0.005
III PART NAME ASSIGNED BY CONTROLLING AGENCY: BENZOCAINE BUTAMBEN AND TETRACAINE HCL TOPICAL AEROSOL 56GM
PRIMARY CONTAINER CONTENT QUANTITY: 56.000 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE, AEROSOL
SPECIAL FEATURES: IN ABLAND WATER SOLUABLE BASE; CONTAINS 0.50 PCT BENZALKONIUM CHLORIDE AND 0.05 PCT CETYL DIMETHYL ETHYL AMMONIUM BROMIDE AS PRESERVATIVES; WITH ONE DETACHABLE,STAINLESS STEEL CANNULA,WHICH,WHEN ATTACHED TO THE PROTRUDING PLASTIC TUBING ON THE
~1: BOTTLE,PERMITS ADMINISTRATION OF ANESTHETIC TO THE DESIRED SITE OF APPLICATION WHEN ACTIVATED
~1: PERCENTAGE W/V CETYL DIMETHYL ETHYL AMMONIUM BROMIDE ACTIVE INGREDIENT

189-7594

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

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189-7594

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

MFG

PATTERSON DENTAL SUPPLY INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 PERCENTAGE, W/V BENZALKONIUM CHLORIDE ACTIVE INGREDIENT AND 14.000 PERCENTAGE, W/V BENZOCAINE ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V BUTAMBEN ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V TETRACAINE HYDROCHLORIDE ACTIVE INGREDIENT AND 0.005
III PART NAME ASSIGNED BY CONTROLLING AGENCY: BENZOCAINE BUTAMBEN AND TETRACAINE HCL TOPICAL AEROSOL 56GM
PRIMARY CONTAINER CONTENT QUANTITY: 56.000 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE, AEROSOL
SPECIAL FEATURES: IN ABLAND WATER SOLUABLE BASE; CONTAINS 0.50 PCT BENZALKONIUM CHLORIDE AND 0.05 PCT CETYL DIMETHYL ETHYL AMMONIUM BROMIDE AS PRESERVATIVES; WITH ONE DETACHABLE,STAINLESS STEEL CANNULA,WHICH,WHEN ATTACHED TO THE PROTRUDING PLASTIC TUBING ON THE
~1: BOTTLE,PERMITS ADMINISTRATION OF ANESTHETIC TO THE DESIRED SITE OF APPLICATION WHEN ACTIVATED
~1: PERCENTAGE W/V CETYL DIMETHYL ETHYL AMMONIUM BROMIDE ACTIVE INGREDIENT

CETACAINE SPRAY

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

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CETACAINE SPRAY

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

MFG

CETYLITE INDUSTRIES INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 PERCENTAGE, W/V BENZALKONIUM CHLORIDE ACTIVE INGREDIENT AND 14.000 PERCENTAGE, W/V BENZOCAINE ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V BUTAMBEN ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V TETRACAINE HYDROCHLORIDE ACTIVE INGREDIENT AND 0.005
III PART NAME ASSIGNED BY CONTROLLING AGENCY: BENZOCAINE BUTAMBEN AND TETRACAINE HCL TOPICAL AEROSOL 56GM
PRIMARY CONTAINER CONTENT QUANTITY: 56.000 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE, AEROSOL
SPECIAL FEATURES: IN ABLAND WATER SOLUABLE BASE; CONTAINS 0.50 PCT BENZALKONIUM CHLORIDE AND 0.05 PCT CETYL DIMETHYL ETHYL AMMONIUM BROMIDE AS PRESERVATIVES; WITH ONE DETACHABLE,STAINLESS STEEL CANNULA,WHICH,WHEN ATTACHED TO THE PROTRUDING PLASTIC TUBING ON THE
~1: BOTTLE,PERMITS ADMINISTRATION OF ANESTHETIC TO THE DESIRED SITE OF APPLICATION WHEN ACTIVATED
~1: PERCENTAGE W/V CETYL DIMETHYL ETHYL AMMONIUM BROMIDE ACTIVE INGREDIENT