Label: CLOROX HAND SANITIZER GEL- alcohol hand sanitizer gel

  • NDC Code(s): 80714-034-01, 80714-034-02, 80714-034-03, 80714-034-04, view more
    80714-034-05, 80714-034-06, 80714-034-08, 80714-034-09, 80714-034-10, 80714-034-11
  • Packager: New Wave Global Services Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 27, 2023

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  • SPL UNCLASSIFIED SECTION

    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.

  • Active Ingredient(s)

    Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Use

    Hand Sanitizer to help reduce bacteria on the skin.

  • Warnings

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

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients

    Water, Acrylates/Vinyl Isodecanoate Crosspolymer (10000 MPA.S Neutralized at 0.5%), Aloe Vera Leaf Extract, Propylene Glycol, Isopropyl Myristate, Fragrance, Vitamin E Acetate, Yellow 10, Yellow 5, Blue 1

  • Questions?

    1-888-325-6769 24 hours, 7 days per week

    www.cloroxhandsanitizer.com

  • Package Label - Principal Display Panel

    CLOROX Hand Sanitizer Gel 12 Oz Bottle-NDC: 80714-034-10

    Clorox Hand Sanitizer Gel 8 Oz Bottle-NDC: 80714-034-09

    clorox HS 4OZx12 Carton, NDC:80714-034-04

    CLOROX HS 4OZX12 CARTON

    CLOROX HS 4OZ Tube, NDC: 80714-034-02

    Clorox HS 4OZ Tube

    CLOROX HS Gallon Jug- NDC 80714-034-08

    CLOROX HS Gallon Jug

    CLOROX HS Pouch-NDC 80714-034-05 Clorox HS Pouch- NDC 80714-034-05

    CLOROX HS 24x Single Use Pouches Carton- NDC 80714-034-06 24x Single Use Pouces Carton NDC 80714-034-06

    CLOROX HS 12X2oz Tube Display Carton- NDC 80714-034-03 12x2 oz Tubes Display Carton

    CLOROX HS 2OZ Tube-NDC 80714-034-01

    Clorox Hand Sanitizer Gel - 2oz Tube Label NDC: 80714-034-01

    6 x 12 oz Bottles

    6 x 12 oz Bottles

  • INGREDIENTS AND APPEARANCE
    CLOROX HAND SANITIZER GEL 
    alcohol hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80714-034
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE (UNII: V5VD430YW9)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80714-034-0312 in 1 CARTON10/30/202002/28/2023
    1NDC:80714-034-0159 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:80714-034-083780 mL in 1 JUG; Type 0: Not a Combination Product01/20/202101/31/2025
    3NDC:80714-034-0624 in 1 CARTON01/20/202101/31/2023
    3NDC:80714-034-053 mL in 1 POUCH; Type 0: Not a Combination Product
    4NDC:80714-034-09236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/25/202102/29/2024
    5NDC:80714-034-116 in 1 CARTON10/30/202003/31/2024
    5NDC:80714-034-10354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    6NDC:80714-034-0412 in 1 CARTON10/30/202003/31/2024
    6NDC:80714-034-02118 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/30/202001/31/2025
    Labeler - New Wave Global Services Inc (202806733)
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