Label: HI AND DRI ROLL ON- aluminum chlorohydrate liquid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 10967-600-17, 10967-602-17 - Packager: Revlon Consumer Products Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated November 10, 2016
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- ACTIVE INGREDIENT
- Purpose
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HI AND DRI ROLL ON
aluminum chlorohydrate liquid liquidProduct 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 liquidProduct 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)
Hi & Dri Roll-On Antiperspirant
