HI AND DRI ROLL ON- aluminum chlorohydrate liquid liquid

Hi and Dri Roll On by

Drug Labeling and Warnings

Hi and Dri Roll On by is a Otc medication manufactured, distributed, or labeled by Revlon Consumer Products Corp, REVLON, INC., Revlon South Africa (PTY) Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Aluminum chlorohydrate 18%

Purpose

Antiperspirant

WARNINGS

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.

INACTIVE INGREDIENT

Inactive Ingredients

aqua((water) eau), glyceryl stearate, laureth-23, magnesium aluminum silicate, laureth-4, lauric acid, cetearyl alcohol, behentrimonium methosulfate, edta

INDICATIONS & USAGE

Reduces underarm wetness

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

Hi & Dri Roll-On Antiperspirant

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HI AND DRI ROLL ON 
aluminum chlorohydrate liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-602
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	0.18 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
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)
LINALOOL, (+)- (UNII: F4VNO44C09)
CITRAL (UNII: T7EU0O9VPP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LAURETH-23 (UNII: N72LMW566G)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-602-17	50 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/01/2014

HI AND DRI ROLL ON 
aluminum chlorohydrate liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	0.18 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
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)
LINALOOL, (+)- (UNII: F4VNO44C09)
CITRAL (UNII: T7EU0O9VPP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LAURETH-23 (UNII: N72LMW566G)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-600-17	50 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/01/2014

Labeler - Revlon Consumer Products Corp (788820165)

Registrant - REVLON, INC. (188442578)

Establishment
Name	Address	ID/FEI	Business Operations
Revlon South Africa (PTY) Ltd		637155859	manufacture(10967-600, 10967-602)