CLOROX HAND SANITIZER- alcohol gel 
Brand Buzz 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

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

Other information

Inactive ingredients

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

Package Labeling:2ml

LabelBox

Package Labeling:500ml

Label2

Package Labeling:1000ml

Label4

Package Labeling:1000ml Refill

Bottle

CLOROX HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69540-0025
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69540-0025-1100 in 1 BOX03/19/2021
12 mL in 1 PACKET; Type 0: Not a Combination Product
2NDC:69540-0025-2500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/19/2021
3NDC:69540-0025-31000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/19/2021
4NDC:69540-0025-41000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/19/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/19/2021
Labeler - Brand Buzz LLC (079266204)
Establishment
NameAddressID/FEIBusiness Operations
Shenzhen Lantern Science Co. Ltd.421222423manufacture(69540-0025)
Establishment
NameAddressID/FEIBusiness Operations
Zhejiang Guoyao Jingyue Aerosol Co., Ltd.554529812manufacture(69540-0025)

Revised: 2/2023
Document Id: f3bfb61d-b5c7-815a-e053-2a95a90a3f92
Set id: bdd47d2f-5332-1430-e053-2a95a90a1c33
Version: 2
Effective Time: 20230202
 
Brand Buzz LLC