Label: CVS PHARMACY- ethyl alcohol liquid

  • 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 December 17, 2009

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

  • Active Ingredient

    Ethyl Alcohol 70% (Antimicrobial)

  • Keep out of reach of children

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately

  • Uses

    To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

  • Questions? comments?

    1-800-shop-CVS (1-800-746-7287)

  • Stop using this product and ask a doctor

    if irritation or rash develops and lasts

  • When using this product

    • Avoid contact with eyes. If contact occurs, rinse eye throughly with water.
    • Pump enough foam in your palm to throughly cover your hands. Rub hands together briskly until dry.
    • Children under 6 years of age should be supervised when using this product.
  • Warnings

    • For external use only
    • Flammable, keep away from heat or flame.


  • PACKAGE FRONT AND BACK LABELS

    1. 8OZ (MM1) Labels8.jpg
      8OZ FRONT AND BACK LABELS
    2. 2OZ (MM2) Labels2.jpg
      2OZ FRONT AND BACK LABELS





  • INGREDIENTS AND APPEARANCE
    CVS PHARMACY   FOAM HAND SANITIZER WITH ALOE
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-252
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 28.8795 mL  in 100 mL
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC) 1.0 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.0001 mL  in 100 mL
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) 0.0001 mL  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) 0.02 mL  in 100 mL
    PROPYLENE OXIDE (UNII: Y4Y7NYD4BK) 0.02 mL  in 100 mL
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.0001 mL  in 100 mL
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.0001 mL  in 100 mL
    FD&C RED NO. 40 (UNII: WZB9127XOA) 0.0001 mL  in 100 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) 0.02 mL  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) 0.02 mL  in 100 mL
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) 0.02 mL  in 100 mL
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 0.02 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63148-252-0250 mL in 1 BOTTLE, PLASTIC
    2NDC:63148-252-08236 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33312/17/2009
    Labeler - Apollo Health and Beauty Care (201901209)