Label: HANDSANITIZERGELBLOODORANGE- gc-hand sanitizer gel-blood orange gel

  • NDC Code(s): 72496-1130-1, 72496-1130-2
  • Packager: Naturich Labs, Inc
  • 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 23, 2023

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  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses:

    Helps decrease bacteria on skin. Recommended for repeated use

  • Warnings

    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

  • Stop Use

    Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours.

  • Keep out of reach of children.

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

  • Directions:

    Squeeze a small drop onto palms and rub together. For children under 6 years, use adult supervision. Not recommended for infants.

  • Inactive Ingredients:

    Water (Aqua), Propanediol, Aloe Barbadensis (Aloe Vera) Leaf Juice, Caprylic/Capric Triglyceride, Cocos Nucifera (Coconut) Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Lavandula Angustifolia (Lavender) Flower Extract, Natural Fragrance*, Aminomethyl Propanol, Carbomer, Citrus Aurantium Bergamia (Bergamo!) Fruit Oil, Tocopheryl Acetate, Citral, Limonene, Linalool.

  • Other Information:

    Store between 16-30C (59-86F).

    Avoid freezing and excessive heat above 40C (104F)

  • PRINCIPAL DISPLAY PANEL

    GC Sanitizer Gel Back Panel

  • INGREDIENTS AND APPEARANCE
    HANDSANITIZERGELBLOODORANGE 
    gc-hand sanitizer gel-blood orange gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72496-1130
    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
    WATER (UNII: 059QF0KO0R) 32 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72496-1130-159.1 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/21/2020
    2NDC:72496-1130-2221.8 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/21/2020
    Labeler - Naturich Labs, Inc (124281663)
    Registrant - Naturich Labs, Inc (124281663)
    Establishment
    NameAddressID/FEIBusiness Operations
    Naturich Labs, Inc124281663manufacture(72496-1130)
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