Label: AROMATIQUE APRICOT MINT HAND SANITIZER- alcohol spray

  • NDC Code(s): 66902-710-02
  • Packager: Natural Essentials, 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 September 10, 2020

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

  • Active Ingredients

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • USES

    For hand washing to decrease bacteria on skin.

  • Warnings

    Flammable. Keep away from fire or flame. For external use only.

    WHEN USING THIS PRODUCT

    Do not use in eyes. In case of contact with eyes, rinse with water.

    STOP USE AND ASK A DOCTOR IF

    Irritation and redness develop and persist.

    KEEP OUT OF REACH OF CHILDREN.

    If swallowed, get medical help promptly.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Other Information

    Store under 105°F

  • Inactive Ingredients

    Aloe Barbadensis Leaf, Dimethicone, Fragrance, Water

  • Principal Display Panel – Bottle Label

    AROMATIQUE®

    / No. 20

    Apricot Mint

    /

    SPRAY HAND SANITIZER

    Spray désinfectant pour les mains

    2 FLUID OZ (59 ml)

    Figure
  • INGREDIENTS AND APPEARANCE
    AROMATIQUE APRICOT MINT HAND SANITIZER 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-710
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol0.70 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66902-710-0259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/10/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/10/2020
    Labeler - Natural Essentials, Inc. (947484713)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURAL ESSENTIALS, INC.947484713MANUFACTURE(66902-710)