CLOROX ANTIMICROBIAL- chloroxylenol soap

Clorox Antimicrobial by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Chloroxylenol 0.5% w/w

Purpose

Antimicrobial

INDICATIONS & USAGE

Uses

• For handwashing to decrease bacteria on the skin
• Ideal for repeated washing

WARNINGS

Warnings

For external use only

WHEN USING

When using this product

• 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
• Apply product
• Wash hands thoroughly
• Rinse vigorously

OTHER SAFETY INFORMATION

Other Information

Store at room temperature

INACTIVE INGREDIENT

Inactive IngredientsCocoamidopropyl Betaine, DMDM Hydantoin, Ethylene Glycol Monostearate, FD&C Blue #1, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, Methylparaben, PEG-120 Methyl Glucose Dioleate, Propylparaben, Sodium Chloride, Sodium Laureth Sulfate, Water.

Questions or Comments?

QUESTIONS OR COMMENTS?

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

PRINCIPAL DISPLAY PANEL

Clorox Antimicrobial Hand Soap

18 oz (532 mL)

INGREDIENTS AND APPEARANCE

CLOROX ANTIMICROBIAL 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 26509-0011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCOL STEARATE (UNII: 0324G66D0E)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
DMDM HYDANTOIN (UNII: BYR0546TOW)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
WATER (UNII: 059QF0KO0R)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 26509-0011-5	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 Co.		007372329	manufacture(26509-0011)