HI AND DRI ROLL ON- aluminum chlorohydrate 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, Inc. 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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-786
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)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
EDTA (UNII: 9G34HU7RV0)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LAURETH-23 (UNII: N72LMW566G)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-786-17	50 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	01/01/2022

Labeler - Revlon Consumer Products Corp (788820165)

Registrant - REVLON, INC. (188442578)

Establishment
Name	Address	ID/FEI	Business Operations
Revlon, Inc		809725570	manufacture(10967-786)