CLOROX ANTIBACTERIAL HAND - WILD LAVENDER AND VANILLA- chloroxylenol soap

Clorox Antibacterial Hand - Wild Lavender and Vanilla by

Drug Labeling and Warnings

Clorox Antibacterial Hand - Wild Lavender and Vanilla by is a Otc medication manufactured, distributed, or labeled by Brand Buzz. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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DRUG FACTS

Active Ingredient

Chloroxylenol (0.3%)

Purpose

Antibacterial hand soap

Uses

• Helps to decrease bacteria on the skin.

Warnings

For external use only.

Keep out of reach of children, except under adult supervision. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions

• Apply onto wet hands, lather for at least 30 seconds and rinse thoroughly.

Inactive Ingredients

WATER (AQUA, EAU), SODIUM LAURETH SULFATE, PEG-4 RAPESEEDAMIDE, PANTHENOL, TOCOPHERYL ACETATE, BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT, COCOS NUCIFERA (COCONUT) FRUIT EXTRACT, COCAMIDOPROPYL BETAINE, PEG-150 DISTEARATE, POLYSORBATE 20, GLYCERIN, ASCORBIC ACID, BIOTIN, NIACINAMIDE, PROPYLENE GLYCOL, SODIUM CHLORIDE, CITRIC ACID, PEG/PPG-18/18 DIMETHICONE, SODIUM HYDROXIDE, TETRASODIUM EDTA, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FRAGRANCE (PARFUM), EXT. VIOLET 2 (CI 60730), RED 33 (CI 17200), ALPHA-ISOMETHYL IONONE, BUTYLPHENYL METHYLPROPIONAL

Questions?

1-855-539-3564

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Distributed by Brand Buzz LLC,
1400 Broadway, New York, NY 10018

PRINCIPAL DISPLAY PANEL - 295 mL Bottle Label

CLOROX™

antibacterial

HAND SOAP
DERMATOLOGIST TESTED

MOISTURIZING

wild lavender
& vanilla

10 FL OZ (295 mL)

INGREDIENTS AND APPEARANCE

CLOROX ANTIBACTERIAL HAND - WILD LAVENDER AND VANILLA 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69540-0075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q)	Chloroxylenol	0.003 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)
PEG-4 Rapeseedamide (UNII: 89575CN928)
Panthenol (UNII: WV9CM0O67Z)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Sheanut Oil (UNII: O88E196QRF)
Coconut (UNII: 3RT3536DHY)
Cocamidopropyl betaine (UNII: 5OCF3O11KX)
PEG-150 Distearate (UNII: 6F36Q0I0AC)
Polysorbate 20 (UNII: 7T1F30V5YH)
Glycerin (UNII: PDC6A3C0OX)
Ascorbic Acid (UNII: PQ6CK8PD0R)
Biotin (UNII: 6SO6U10H04)
Niacinamide (UNII: 25X51I8RD4)
Propylene Glycol (UNII: 6DC9Q167V3)
Sodium Chloride (UNII: 451W47IQ8X)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
PEG/PPG-18/18 Dimethicone (UNII: 9H0AO7T794)
Sodium Hydroxide (UNII: 55X04QC32I)
Edetate Sodium (UNII: MP1J8420LU)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
EXT. D&C Violet NO. 2 (UNII: G5UX3K0728)
D&C Red NO. 33 (UNII: 9DBA0SBB0L)
Isomethyl-.Alpha.-Ionone (UNII: 9XP4LC555B)
Butylphenyl Methylpropional (UNII: T7540GJV69)

Product Characteristics
Color	PURPLE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69540-0075-1	295.735 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	02/01/2016

Labeler - Brand Buzz (079266204)