HI AND DRI ANTIPERSPIRANT ROLL-ON POWDER FRESH- aluminum chlorohydrate 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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Hi & Dri Roll-On Antiperspirant - Powder Fresh 1.7 fl. oz (50 ml)

Drug Facts
Active Ingredient

Aluminum chlorohydrate 18%

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, laureth-4, lauric acid, cetearyl alcohol, behentrimonium methosulfate, edta, alpha-isomethyl ionone, citronellol, limonene, hydroxycitronellol, benzyl alcohol, benzyl salicylate, linalool, citral

Questions

1-800-473-8566

Principal Display Panel - 1.7 fl oz bottle

MM1

HI AND DRI ANTIPERSPIRANT  ROLL-ON POWDER FRESH
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10967-057
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE0.18 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
LAURETH-23 (UNII: N72LMW566G)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
LAURETH-4 (UNII: 6HQ855798J)  
LAURIC ACID (UNII: 1160N9NU9U)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
EDETIC ACID (UNII: 9G34HU7RV0)  
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
GERANIOL (UNII: L837108USY)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
LINALOOL, (+)- (UNII: F4VNO44C09)  
CITRAL (UNII: T7EU0O9VPP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10967-057-9750 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/01/1982
Labeler - Revlon Consumer Products Corp (788820165)
Establishment
NameAddressID/FEIBusiness Operations
Revlon South Africa (PTY) Ltd637155859manufacture(10967-057)

Revised: 12/2013
Document Id: 3222fd3d-5e0c-40ac-ad46-9bef480bafab
Set id: 8a7149f6-2e72-4f49-a265-34747172588e
Version: 1
Effective Time: 20131209
 
Revlon Consumer Products Corp