Label: ALCHEMY LIVING HAND SANITIZER BLACK CHERRY FRAGRANCE- ethyl alcohol liquid

  • 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 April 15, 2023

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

  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • To decrease bacteria on the skin that could cause disease.
    • Recommended for repeated use.

  • Warnings

    For external use only-hands. Flammable. Keep away from heat and flame. When using this product.
    • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
    • Avoid contact with broken skin. • Do not inhale or ingest. Stop use and ask a doctor if skin irritation develops.

    Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • Directions

    • Wet hands thoroughly 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), Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, Propylene Glycol, Vitamin E, Fragrance.

  • SPL UNCLASSIFIED SECTION

    KILLS 99.9% OF GERMS

    Manufactured for and distributed by
    Pearl World Inc, NY, NY 10019 Pearlworldinc.com
    All rights reserved. Designed in the USA. Made in China.

  • Packaging

    SanitizerBlackCherry-440

  • INGREDIENTS AND APPEARANCE
    ALCHEMY LIVING HAND SANITIZER BLACK CHERRY FRAGRANCE 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69933-440
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69933-440-3230 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/14/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/14/2023
    Labeler - Pearl World Inc. (043130142)