Label: EQUATE HAND SANITIZER WITH VITAMIN E- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL

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 June 8, 2020

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  • Active ingredient

    Alcohol Denat. 62%

  • Purpose

    Antiseptic

  • Uses

    ■ to decrease bacteria on the skin that could cause disease ■ recommended for repeated use

  • Warnings

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

  • When using this product

    ■ keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ avoid contact with broken skin ■ do not inhale or ingest

  • Stop use and ask a doctor if

    ■ irritation and redness develop ■ condition persists for more than 72 hours

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    ■ wet hands thoroughly with product and allow to dry without wiping ■ for children under 6, use only under adult supervision ■ not recommended for infants

  • Other information

    ■ do not store above 105ºF ■ may discolor some fabrics ■ harmful to wood finishes and plastics

  • Inactive ingredients

    Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate, Tocopheryl Acetate

  • Questions?

    1-888-287-1915

  • Package Label

    package label

  • INGREDIENTS AND APPEARANCE
    EQUATE HAND SANITIZER  WITH VITAMIN E
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-172
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-172-0150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/11/2020
    2NDC:49035-172-0389 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/11/2020
    3NDC:49035-172-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/11/2020
    4NDC:49035-172-12354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/11/2020
    5NDC:49035-172-30887 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/11/2020
    6NDC:49035-172-341000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/11/2020
    Labeler - Wal-Mart Stores, Inc. (051957769)
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