Label: MOISTURIZING ANTIBACTERIAL- benzalkonium chloride 0.13% soap
- NDC Code(s): 30142-826-03, 30142-826-68, 30142-826-81, 30142-826-96
- Packager: The Kroger Co.,
- 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 August 25, 2023
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- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Inactive ingredients
- Adverse reactions
- Disclaimer
- Principal display panel
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INGREDIENTS AND APPEARANCE
MOISTURIZING ANTIBACTERIAL
benzalkonium chloride 0.13% soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-826 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) SODIUM CHLORIDE (UNII: 451W47IQ8X) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) GLYCERIN (UNII: PDC6A3C0OX) DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SULISOBENZONE (UNII: 1W6L629B4K) SODIUM BENZOATE (UNII: OJ245FE5EU) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-826-96 221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/09/2014 2 NDC:30142-826-68 1656 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/09/2014 3 NDC:30142-826-81 332 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/09/2014 4 NDC:30142-826-03 1478 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/09/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/09/2014 Labeler - The Kroger Co., (006999528) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(30142-826) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(30142-826)