Label: ANTIBACTERIAL WET WIPES- benzalkonium chloride swab
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Contains inactivated NDC Code(s)
NDC Code(s): 76772-008-40 - Packager: TSM ITHALAT IHRACAT SANAYI VE DIS TICARET LIMITED SIRKETI
- Category: HUMAN OTC DRUG LABEL
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 May 7, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Use
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
- Directions
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL WET WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76772-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) 2-METHYL-1,2-BENZOISOTHIAZOLIN-3-ONE (UNII: 81PV9X5Y68) PEG-40 HYDROGENATED LANOLIN (UNII: 959P5CXE48) EDETATE SODIUM (UNII: MP1J8420LU) CITRIC ACID ACETATE (UNII: DSO12WL7AU) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) WATER (UNII: 059QF0KO0R) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76772-008-40 40 in 1 PACKAGE; Type 0: Not a Combination Product 05/07/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/07/2020 Labeler - TSM ITHALAT IHRACAT SANAYI VE DIS TICARET LIMITED SIRKETI (533120570)