CLOROX Hand Sanitizer Gel Tube

CLOROX Hand sanitizer Gel by

Drug Labeling and Warnings

CLOROX Hand sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Span Packaging Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Tube

CLOROX

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.

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

CLOROX HAND SANITIZER GEL 
alcohol hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55049-034
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55049-034-03	12 in 1 CARTON	10/30/2020
1	NDC: 55049-034-01	59 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 55049-034-04	12 in 1 CARTON	01/18/2021
2	NDC: 55049-034-02	118 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/30/2020

Labeler - Span Packaging Services LLC (557434805)

Establishment
Name	Address	ID/FEI	Business Operations
Span Packaging Services LLC		557434805	manufacture(55049-034) , pack(55049-034) , label(55049-034)

Revised: 6/2022

Document Id: e2342e66-17a6-7dd2-e053-2a95a90a6f9f

34390-5

Set id: 6d6135de-e2d0-40d6-9c85-c5a5c8901694

Version: 3

Effective Time: 20220624