Label: CVS PHARMACY- benzalkonium chloride soap
- NDC Code(s): 51316-704-07, 51316-704-32
- Packager: CVS Pharmacy Inc
- 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 31, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Water( Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis, Leaf Juice, Cocos Nucifera (Coconut) Fruit Extract, Bambusa Vulgaris Extract, Propylene Glycol, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone -4, Methylcholoroisothiazolinone, Methylisothiazolinone, Blue 1 (Cl 42090), Red 33 (Cl 17200)
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CVS PHARMACY
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-704 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 130 mg in 100 mL Inactive Ingredients Ingredient Name Strength DECYL GLUCOSIDE (UNII: Z17H97EA6Y) HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM CITRATE (UNII: 1Q73Q2JULR) SULISOBENZONE (UNII: 1W6L629B4K) POLYSORBATE 20 (UNII: 7T1F30V5YH) FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF) BAMBUSA VULGARIS LEAF (UNII: EMY54R518C) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) D&C RED NO. 33 (UNII: 9DBA0SBB0L) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ALOE VERA LEAF (UNII: ZY81Z83H0X) COCOS NUCIFERA WHOLE (UNII: 245J88W96L) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-704-07 222 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/15/2022 2 NDC:51316-704-32 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/15/2022 Labeler - CVS Pharmacy Inc (062312574) Registrant - Apollo Health and Beauty Care Inc (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care Inc. 201901209 manufacture(51316-704)