CLOROX CARE CONCEPTS ANTIMICROBIAL- benzalkonium chloride soap

Clorox Care Concepts Antimicrobial by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.12%

Purpose

Antiseptic handwash

Use

• For handwashing to decrease bacteria on skin that potentially can cause disease
• Recommended for repeated use

Warnings

For external use only.

WHEN USING

When using this product, do not use in the eyes.

STOP USE

Discontinue use and ask a doctor if

• irritate and redness develop.
• condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• Wet hands and forearms.
• Dispense onto hands.
• Scrub thoroughly for 30 seconds.
• Rinse and repeat.

Inactive ingredients

Benzyl Alcohol, Citric Acid, Cocamidopropyl Betaine, Dehydroacetic Acid, Glycerin, Phenoxyethanol, Poloxamer 124, Sodium Hydroxide, Tetra Sodium EDTA, Water

PRINCIPAL DISPLAY PANEL

Clorox Care Concepts

Antimicrobial Soap

INGREDIENTS AND APPEARANCE

CLOROX CARE CONCEPTS ANTIMICROBIAL 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 26509-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.12 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLOXAMER 124 (UNII: 1S66E28KXA)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 26509-0003-1	44 mL in 1 BOTTLE, PUMP
2	NDC: 26509-0003-2	249 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2014

Labeler - The Clorox Company (009138033)

Registrant - The Clorox Company (009138033)