Label: HAND SANITIZER- alcohol gel

  • 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 July 3, 2020

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  • Active ingredient

    Alcohol Denat 62%

  • Purpose

    Antiseptic

  • Use

    ■ For handwashing to decrease bacteria on the skin ■ Recommended for repeated use

  • Warnings

    ■ For external use only

    ■ Flammable, keep away from fire & flame

    ■ Does not contain grain alcohol;do not drink. If taken internally will produce serious gastric disturbances.

  • When using this product

    ■ Avoid the eyes and mucous membranes ■ In the case of eyes or mucous membrane contact, rinse area thoroughly with water

  • Stop use and ask a doctor if

    ■ Condition worsens

    ■ Redness or irritation develops

    ■ If condition persists for more than 3 days

  • Keep out of reach of children

    ■ If swallowed contact a doctor or Poison Control Center immediately.

  • Directions

    ■ Rub dime sized amount between hands until dry

    ■ Supervise children in the use of this product

    ■ In the case of eye contact, rinse eyes thoroughly with water

  • Other information

    ■ Store below 105°F

    ■ May discolor some fabrics

  • Inactive Ingredients

    Water, Fragrance, PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate, D&C Red No. 33(CI 17200)

  • Questions?

    ■ 1-800-278-9218

  • Package Label

    package label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49852-602
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49852-602-3030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2020
    Labeler - Tri-Coastal Design Company Inc. (609734900)
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