Label: WIPE OUT ANTIBACTERIAL LIQUID HAND COCONUT VANILLA- benzalkonium chloride soap
-
Contains inactivated NDC Code(s)
NDC Code(s): 77878-027-01 - Packager: TZUMI INNOVATIONS LLC
- 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 December 23, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WIPE OUT ANTIBACTERIAL LIQUID HAND COCONUT VANILLA
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77878-027 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) D&C RED NO. 7 (UNII: ECW0LZ41X8) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) DISODIUM HEDTA (UNII: KME849MC7A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77878-027-01 221 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/23/2020 Labeler - TZUMI INNOVATIONS LLC (117426322) Establishment Name Address ID/FEI Business Operations Aogrand International Trade Corporation 421353092 manufacture(77878-027)