CLOROX ANTIMICROBIAL HAND SANITIZER- ethyl alcohol gel 
The Clorox Company

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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Drug Facts

Ethyl Alcohol 62% w/w

Antimicrobial

Uses

• To sanitize hands without requiring water or a rinse

Warnings

FLAMMABLE

For external use only

When using this product

• do not use near heat or flame

• do not use in or near eyes

• discontinue use if irritation and redness develop, or if condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

• Wet hands thoroughly with product and allow to dry without wiping

Other Information

• Store at room temperature

Inactive ingredients

QUESTIONS OR COMMENTS?

Call 1-800-638-2625 or visit www.hlk.cc

Clorox Antimicrobial Hand Sanitizer

18 FL OZ (532 mL) CLX Blue Hand Sanitizer

CLOROX ANTIMICROBIAL HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:26509-0010-8532 mL in 1 BOTTLE; Type 0: Not a Combination Product01/25/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/25/2016
Labeler - The Clorox Company (009138033)
Registrant - Carroll Company (007372329)
Establishment
NameAddressID/FEIBusiness Operations
Carroll Company007372329manufacture(26509-0010)

Revised: 1/2016
Document Id: 2561abfd-61dc-562c-e054-00144ff8d46c
Set id: 2561c0da-3cf8-58b9-e054-00144ff88e88
Version: 1
Effective Time: 20160125
 
The Clorox Company