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

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Benzalkonium Chloride

  • PURPOSE

    Hand washing

  • WARNINGS

    For External Use Only

    Avoid contact with eyes. In case of contact, rinse throughly with water.

    Ask a doctor if: Irritation or redness develops and lasts

    In case of accidental ingestion, seek medical attention or contact a poison control centre immediately.

  • DOSAGE & ADMINISTRATION

    Apply onto dry hands, work into a lather, rinse and dry throughly.

  • STORAGE AND HANDLING

    Store at room temperature.

  • 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

    Helps eliminate bacteria on the skin

  • PRINCIPAL DISPLAY PANEL

    7.5oz32oz

  • INGREDIENTS AND APPEARANCE
    CVS PHARMACY 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-704
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE130 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51316-704-07222 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2022
    2NDC:51316-704-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/15/2022
    Labeler - CVS Pharmacy Inc (062312574)
    Registrant - Apollo Health and Beauty Care Inc (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care Inc.201901209manufacture(51316-704)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!