CLOROX HAND SANITIZER- alcohol gel

Clorox Hand Sanitizer by

Drug Labeling and Warnings

Clorox Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Brand Buzz LLC, Shenzhen Lantern Science Co. Ltd., Zhejiang Guoyao Jingyue Aerosol Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 71% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Warnings

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

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Discontinue use

if irritation and redness develop. If condition persists for more than 72 hours consult a physician.

Keep out of reach of children.

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

Directions

• Squeeze gel into your palm and briskly rub hands together until dry.
• Children under 6 years of age should be supervised when in use.

Other information

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

Inactive ingredients

Aloe Barbadensis Leaf Extract, Carbomer, Glycerin, Tocopheryl Acetate (Vitamin E), Triethanolamine, Water (Aqua).

Package Labeling:2ml

Package Labeling:500ml

Package Labeling:1000ml

Package Labeling:1000ml Refill

INGREDIENTS AND APPEARANCE

CLOROX HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69540-0025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69540-0025-1	100 in 1 BOX	03/19/2021
1		2 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 69540-0025-2	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2021
3	NDC: 69540-0025-3	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2021
4	NDC: 69540-0025-4	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/19/2021

Labeler - Brand Buzz LLC (079266204)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co. Ltd.		421222423	manufacture(69540-0025)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Guoyao Jingyue Aerosol Co., Ltd.		554529812	manufacture(69540-0025)