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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Womens Mitchum Advanced Roll On Antiperspirant Deodorant

Drug Facts
Active Ingredient

Aluminum zirconium tetrachlorohydrex gly 20%

Purpose

Antiperspirant

Use

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

MM1

WOMENS MITCHUM ADVANCED INVISIBLE  ROLL-ON ANTIPERSPIRANT DEODORANT POWDER FRESH
aluminum zirconium tetrachlorohydrex gly liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10967-583
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY0.20 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10967-583-9750 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35012/15/2013
Labeler - Revlon Consumer Products Corp (788820165)
Establishment
NameAddressID/FEIBusiness Operations
Revlon South Africa (PTY) Ltd637155859manufacture(10967-583)

Revised: 12/2013
Document Id: 50ea516c-c1a6-4f98-bce9-ddcec2da99a9
Set id: 0cbbcbe8-f434-488b-b9f4-4aec904dfb38
Version: 1
Effective Time: 20131205
 
Revlon Consumer Products Corp