Label: AMORA HAND SANITIZER COCONUT- alcohol spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 27, 2026

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70% v/v

    Purpose

    Antibacterial

  • Uses

    • For hand-washing to decrease bacteria on the skin.
  • Warnings

    For external use only.

    Flammabel, keep away from fire and flames

    when using this product

    • test on a small area of skin before full use.
    • keep out of eyes. In case of contact with eyes, flush throughly with water.
    • Avoid contact with broken skin.
    • Do not inhale or ingest.

    Stop use and ask doctor if

    • allergy, irritation or redness develops.
    • Condition persists for more than 72 hours.

    Keep out of reach of children.

    • If product is swallowed, get medical help or contact a poison control centre right away.
  • Directions

    • Spray hands 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 105° F
    • May discolor some fabrics
    • Harmful to wood finishes and plastics
  • Inactive ingredients

    WATER (AQUA), FRAGRANCE (PARFUM), COCOS NUCIFERA COCONUT WATER, BUTYLENE GLYCOL, HYDROXYACETOPHENONE.

  • Questions or comments?

    1-212-244-5170  info@amora.beauty

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    AMORA HAND SANITIZER COCONUT 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85179-038
    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
    COCOS NUCIFERA WHOLE (UNII: 245J88W96L)  
    WATER (UNII: 059QF0KO0R)  
    COCONUT WATER (UNII: 267F5Y81NT)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85179-038-0045 mL in 1 BOTTLE; Type 0: Not a Combination Product11/17/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/17/2025
    Labeler - I World LLC (830590126)
    Registrant - I World LLC (830590126)
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