Label: CARE PLUS HAND SANITIZER- ethyl 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 June 22, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70.0% v/v

  • Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    Uses hand sanitizer to help reduce bacteria on the skin.

  • Warnings

    For external use only.

    Flammable. Keep away from heat and flame.

    When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

    Stop use and ask a doctor if irritation or redness develops.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

  • DOSAGE & ADMINISTRATION

    Directions ▪ wet hands thoroughly with product and rub into skin until dry.▪ Children under 6 years of age should be supervised by an adult. when using this product.

  • INACTIVE INGREDIENT

    Inactive ingredients Water, Aloe Barbadensis Leaf Juice, Carbomer,Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine

  • SPL UNCLASSIFIED SECTION

    KILLS GERMS*

    ANTIBACTERIAL

    with Moisturizers & Vitamin E

    *Kills 99.9% of many common germs.

    www.ostltrade.com

    Imported by O.S.T.L.Inc

    Made in P.R.C.

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    CARE PLUS HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69950-028
    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)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69950-028-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/17/2020
    Labeler - Ostl, Inc. (020117798)
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