Label: SATURDAY SKIN HAND SANITIZING MIST- hand sanitizing mist spray

  • 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 November 16, 2020

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

  • ACTIVE INGREDIENT

    Alcohol 65% v/v - purpose: Antimicrobial

  • PURPOSE

    Purpose: Antimicrobial

  • INDICATIONS & USAGE

    Hand Sanitizer to help reduce bacteria that potentially can cause disease

  • WARNINGS

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

  • WHEN USING

    Do not use in or near the eyes, ears, and mouth. In case of contact, rinse thoroughly with water. Do not use in the mouth, mucous membrane, or open skin wound as it may cause irritation. Take precaution when using if allergic to Propylene Glycol.

  • STOP USE

    and ask a doctor if irritation or rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Spray once in the hand

  • OTHER SAFETY INFORMATION

    Store between 15˚C to 30˚C (59˚F to 86˚F), Avoid freezing and excessive heat above 40˚C (104˚F)

  • INACTIVE INGREDIENT

    Water, Glycerin, Citrus Nobilis (Mandarin Orange) Peel Oil, PEG-60 Hydrogenated Castor Oil, PEG-40 Hydrogenated Castor Oil, Rosmarinus Officinalis (Rosemary) Extract, Aloe Barbadensis Leaf Extract, Gardenia Jasminoides Fruit Extract, Camellia Sinensis Leaf Extract

  • QUESTIONS

    213-487-3211

  • PRINCIPAL DISPLAY PANEL

    ​30 mL NDC 80746-100-01

    Saturday Skin Sanitizing Mist

  • INGREDIENTS AND APPEARANCE
    SATURDAY SKIN HAND SANITIZING MIST 
    hand sanitizing mist spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80746-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 65 mL
    Inactive Ingredients
    Ingredient NameStrength
    MANDARIN OIL (UNII: NJO720F72R)  
    ROSEMARY (UNII: IJ67X351P9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80746-100-0130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/18/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/18/2020
    Labeler - CHALOGY, INC. (080272002)
    Establishment
    NameAddressID/FEIBusiness Operations
    E.CIS COSMETIC.,Co.Ltd689846270manufacture(80746-100)