Label: ANTIBACTERIAL- benzalkonium chloride 0.13% soap
- NDC Code(s): 11673-633-68, 11673-633-96
- Packager: Target Corp
- 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 March 22, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- disclaimer
- Active ingredients
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
-
inactive ingredientsc
water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, myristamidopropylamine oxide, glycerin,
fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate,
Citrus nobilis (mandarin orange) oil, Camellia sinensis leaf extract, Zingiber officinale (ginger) root oil, blue 1, yellow 5
- Adverse Reactions
- principal display panel
-
INGREDIENTS AND APPEARANCE
ANTIBACTERIAL
benzalkonium chloride 0.13% soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-633 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 g 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) EDETATE SODIUM (UNII: MP1J8420LU) SULISOBENZONE (UNII: 1W6L629B4K) SODIUM BENZOATE (UNII: OJ245FE5EU) MANDARIN OIL (UNII: NJO720F72R) GREEN TEA LEAF (UNII: W2ZU1RY8B0) GINGER OIL (UNII: SAS9Z1SVUK) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-633-96 221.8 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/15/2015 2 NDC:11673-633-68 1656 mL in 1 PACKAGE; Type 0: Not a Combination Product 04/15/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/15/2015 Labeler - Target Corp (006961700) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(11673-633) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(11673-633)