Label: ANTIMICROBIAL FOAMING SANITIZER- benzethonium chloride liquid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37945-718-14 - Packager: Bio-Medical & Pharmaceutical Manufacturing Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 6, 2018
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- DRUG FACTS
- Active Ingredient
- PURPOSE
- Inactive Ingredients
- Purpose
- Use
- Warnings
- Keep Out Of Reach Of Children
- Other Information
- QUESTIONS
- Directions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIMICROBIAL FOAMING SANITIZER
benzethonium chloride liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37945-718 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.2 g in 100 g Inactive Ingredients Ingredient Name Strength PROPYLPARABEN (UNII: Z8IX2SC1OH) LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) 2-HEXENAL PROPYLENE GLYCOL ACETAL, (1E)- (UNII: ZBS49DF5S4) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) METHYLPARABEN (UNII: A2I8C7HI9T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37945-718-14 207 g in 1 BOTTLE; Type 0: Not a Combination Product 10/09/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/09/2015 Labeler - Bio-Medical & Pharmaceutical Manufacturing Corporation (072186356) Establishment Name Address ID/FEI Business Operations Bio-Medical & Pharmaceutical Manufacturing Corporation 072186356 manufacture(37945-718)