Label: NEUTRACETT ALL PURPOSE- allantoin glycerin gel
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Contains inactivated NDC Code(s)
NDC Code(s): 51435-003-01 - Packager: ADVANCED BIOMEDICS INC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated November 9, 2010
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- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
NEUTRACETT ALL PURPOSE
allantoin glycerin gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51435-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.5 mg in 0.1 g GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 50 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYALURONIC ACID (UNII: S270N0TRQY) PANTHENOL (UNII: WV9CM0O67Z) PPG-5-CETETH-20 (UNII: 4AAN25P8P4) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) BENZOIC ACID (UNII: 8SKN0B0MIM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51435-003-01 28.3 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 05/28/2010 Labeler - ADVANCED BIOMEDICS INC (023307026) Registrant - ADVANCED BIOMEDICS INC (023307026) Establishment Name Address ID/FEI Business Operations COSMETIC ENTERPRISES LTD 017701475 manufacture