Label: PERSONAL CARE ANTIBACTERIAL HAND- chloroxylenol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72133-151-15, 72133-151-75 - Packager: Delta Brands & Products LLC
- 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 April 19, 2018
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- Official Label (Printer Friendly)
- 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
- Package Label
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INGREDIENTS AND APPEARANCE
PERSONAL CARE ANTIBACTERIAL HAND
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72133-151 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6) WATER (UNII: 059QF0KO0R) FD&C RED NO. 40 (UNII: WZB9127XOA) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) AMMONIUM CHLORIDE (UNII: 01Q9PC255D) DMDM HYDANTOIN (UNII: BYR0546TOW) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72133-151-75 221.8 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/16/2018 2 NDC:72133-151-15 444 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/16/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/16/2018 Labeler - Delta Brands & Products LLC (080999173)