WOMENS MITCHUM ADVANCED INVISIBLE ROLL-ON ANTIPERSPIRANT DEODORANT POWDER FRESH- aluminum zirconium tetrachlorohydrex gly liquid

Womens Mitchum Advanced Invisible by

Drug Labeling and Warnings

Womens Mitchum Advanced Invisible by is a Otc medication manufactured, distributed, or labeled by Revlon Consumer Products Corp, Revlon South Africa (PTY) Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active Ingredient

Aluminum zirconium tetrachlorohydrex gly 20%

Purpose

Antiperspirant

Use

• Reduces underarm wetness

Warnings:

For external use only.

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irriation occurs

Keep out of reach of children.

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

Directions

Apply to underarms only.

Inactive Ingredients

aqua((water) eau), glyceryl stearate, laureth-23, magnesium aluminum silicate, polysorbate 20, tocopheryl acetate, aloe barbadensis leaf extract, hydrogen peroxide, silica dimethicone silylate, laureth-4, behentrimonium methosulfate, cetearyl alcohol, lauric acid, EDTA, fragrance, benzyl salicylate, linalool, limonene, hexyl cinnamal, coumarin, citronellol, geraniol

Questions

1-888-8-MITCHUM

Principal Display Panel - 1.7 fl oz bottle

INGREDIENTS AND APPEARANCE

WOMENS MITCHUM ADVANCED INVISIBLE  ROLL-ON ANTIPERSPIRANT DEODORANT POWDER FRESH
aluminum zirconium tetrachlorohydrex gly liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-583
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE)	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	0.20 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LAURETH-23 (UNII: N72LMW566G)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
LAURETH-4 (UNII: 6HQ855798J)
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
LAURIC ACID (UNII: 1160N9NU9U)
EDETIC ACID (UNII: 9G34HU7RV0)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
LINALOOL, (+)- (UNII: F4VNO44C09)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
COUMARIN (UNII: A4VZ22K1WT)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-583-97	50 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	12/15/2013

Labeler - Revlon Consumer Products Corp (788820165)

Establishment
Name	Address	ID/FEI	Business Operations
Revlon South Africa (PTY) Ltd		637155859	manufacture(10967-583)