Label: CHLORHEXIDINE GLUCONATE solution
- NDC Code(s): 51072-048-01
- Packager: Aurora Pharmaceutical, Inc.
- Category: OTC ANIMAL DRUG LABEL
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Drug Label Information
Updated February 23, 2023
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- INDICATIONS
- ACTIVE INGREDIENT
- DIRECTIONS FOR USE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- STORAGE
- OTHER INGREDIENTS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1 Gallon Bottle Label
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INGREDIENTS AND APPEARANCE
CHLORHEXIDINE GLUCONATE
chlorhexidine gluconate solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51072-048 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 20 g in 1 L Product Characteristics Color green Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51072-048-01 4 in 1 CARTON 1 3.79 L in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/31/2012 Labeler - Aurora Pharmaceutical, Inc. (832848639) Establishment Name Address ID/FEI Business Operations Aurora Pharmaceutical, Inc. 832848639 manufacture