Label: HAND SANTISER 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 May 14, 2020

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

  • SPL UNCLASSIFIED SECTION

    This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

    The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

    1. Isopropyl Alcohol (75%, v/v) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
    2. Glycerol (1.45% v/v).
    3. Hydrogen peroxide (0.125% v/v).
    4. Sterile distilled water or boiled cold water.

    The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

  • Active Ingredient(s)

    Ethyl Alchol 75%(antiseptic)

  • Purpose

    /

  • Use

    /

  • Warnings

    FOR EXTERNAL USE ONLY
    Avoid contact with eyes. If eye contact occurs, flush with water. Keep out of direct sunligh.

  • Do not use

    /

  • WHEN USING

    /

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Directions

    pump onto gands, latre vigorously for at least 15 seconds, rinse&dry throughly.

  • Inactive ingredients

    Water, TriethanolamineCarbomer, ALoe vera Gel, Fragrance, Glycerol, Propylene, Glycol, VitaminE

  • Package Label - Principal Display Panel

    500302501000500060100/

  • INGREDIENTS AND APPEARANCE
    HAND SANTISER 
    hand santiser gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76881-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    1-O-(2-METHOXY-4-HEXADECENYL)GLYCEROL (UNII: 3A7RDO6AC4)  
    .ALPHA.-TOCOPHEROL SUCCINATE, DL- (UNII: 7VJE08U49E)  
    DETOSU/TRIETHYLENE GLYCOL/TRIETHYLENE GLYCOL POLYGLYCOLIDE COPOLYMER (UNII: JC2Q67KRW7)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    3-(P-METHOXYPHENYL)PROPYLENE-1,2-OXIDE (UNII: 7K4661R4JM)  
    FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER 1342 (UNII: 809Y72KV36)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76881-005-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    2NDC:76881-005-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    3NDC:76881-005-03100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    4NDC:76881-005-04250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    5NDC:76881-005-05500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    6NDC:76881-005-061000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    7NDC:76881-005-075000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/30/2020
    Labeler - Yiwu city jieyi cleaning supplies co., LTD (413161069)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yiwu city jieyi cleaning supplies co., LTD413161069manufacture(76881-005)