CLOROX HAND SANITIZER GEL- alcohol hand sanitizer gel 
Span Packaging Services LLC

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.

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CLOROX Hand Sanitizer Gel

Bottle, Pump

Hand Sanitizer Gel

Kills 99.9% of Common Germs

with Aloe

Contains moisturizers

Bleach-Free

Active Ingredient(s)

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

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. 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.

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

Other information

  • Store between 15-30ºC (59-86ºF)
  • Avoid freezing and excessive heat above 40ºC (104ºF)

Questions?

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

image description

CLOROX HAND SANITIZER GEL 
alcohol hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55049-036
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)  
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)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55049-036-01237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/30/2020
2NDC:55049-036-044 in 1 BOX10/30/2020
2NDC:55049-036-02355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3NDC:55049-036-033785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/30/2020
Labeler - Span Packaging Services LLC (557434805)
Establishment
NameAddressID/FEIBusiness Operations
Span Packaging Services LLC557434805manufacture(55049-036) , pack(55049-036) , label(55049-036)

Revised: 6/2022
Document Id: e2701949-dfbd-1cb9-e053-2a95a90a252d
Set id: d96658e0-5c77-421d-892f-5efad6c173e7
Version: 3
Effective Time: 20220627
 
Span Packaging Services LLC