CLOROX ANTIMICROBIAL HAND SANITIZER- ethyl alcohol gel

Clorox Antimicrobial Hand Sanitizer by

Drug Labeling and Warnings

Clorox Antimicrobial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by The Clorox Company, Carroll Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 62% w/w

PURPOSE

Antimicrobial

INDICATIONS & USAGE

Uses

To sanitize hands without requiring water or a rinse

WARNINGS

Warnings

FLAMMABLE

For external use only

WHEN USING

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

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

DOSAGE & ADMINISTRATION

Directions

Wet hands thoroughly with product and allow to dry without wiping

OTHER SAFETY INFORMATION

Other Information

Store at room temperature

INACTIVE INGREDIENT

Inactive ingredients

• Aloe Barbadensis Leaf Juice
• Carbomer
• Diisopropylamine
• FD&C Blue #1
• Fragrance
• Glycerin
• Isopropyl Myristate
• Phenoxyethanol
• Tocopherol Acetate
• Water

QUESTIONS

QUESTIONS OR COMMENTS?

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

PRINCIPAL DISPLAY PANEL

Clorox Antimicrobial Hand Sanitizer

18 FL OZ (532 mL)

INGREDIENTS AND APPEARANCE

CLOROX ANTIMICROBIAL HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 26509-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	620 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 26509-0010-8	532 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/25/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/25/2016

Labeler - The Clorox Company (009138033)

Registrant - Carroll Company (007372329)

Establishment
Name	Address	ID/FEI	Business Operations
Carroll Company		007372329	manufacture(26509-0010)