Label: ALOE FORMULA ANTIBACTERIAL- benzalkonium chloride soap
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Contains inactivated NDC Code(s)
NDC Code(s): 76383-019-08 - Packager: BBC Group Ltd
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated April 27, 2020
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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
ALOE FORMULA ANTIBACTERIAL
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76383-019 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 METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PHENOXYETHANOL (UNII: HIE492ZZ3T) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) EDETATE DISODIUM (UNII: 7FLD91C86K) MAGNESIUM NITRATE (UNII: 77CBG3UN78) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ALOE VERA LEAF (UNII: ZY81Z83H0X) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) GLYCERYL LAURATE (UNII: Y98611C087) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76383-019-08 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/22/2020 Labeler - BBC Group Ltd (421270060) Establishment Name Address ID/FEI Business Operations BBC Group Ltd 421270060 manufacture(76383-019)