CLARINS - ROLL-ON DEODORANT ALUMINUM CHLOROHYDRATE - ANTIPERSPIRANT, LONG-LASTING, ALCOHOL-FREE- aluminum chlorohydrate liquid

CLARINS - ROLL-ON DEODORANT Aluminum Chlorohydrate - Antiperspirant, long-lasting, Alcohol-free by

Drug Labeling and Warnings

CLARINS - ROLL-ON DEODORANT Aluminum Chlorohydrate - Antiperspirant, long-lasting, Alcohol-free by is a Otc medication manufactured, distributed, or labeled by Laboratoires Clarins. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

ALUMINUM CHLOROHYDRATE 14%(Anhydrous) w/w

Purpose

Antiperspirant

Uses:

Reduces underarm perspiration.

: Warnings

For external use only.

Do not use

• on broken skin. 
• Stop use if rash or irritation occurs

Ask a doctor before use

• if you have kidney disease.

Stop use and ask a doctor

• if skin irritation or sensitivity develops or increases.

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 Ingredient:

WATER . DIPROPYLENE GLYCOL . METHYL GLUCETH-20 . FRAGRANCE . PEG-40 HYDROGENATED CASTOR OIL . HYDROXYETHYLCELLULOSE . BUTYLENE GLYCOL . POLYSORBATE 20 . GLYCERIN . PHENOXYETHANOL . DISODIUM EDTA . ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT . HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT . BAROSMA BETULINA LEAF EXTRACT. [C0493C]

Other information:

Store at 20-25°C (68-77°F)

Questions or comments?

Call 1-866-252-7467 Monday-Friday, 8 a.m. to 5 p.m.

Package Labeling:

INGREDIENTS AND APPEARANCE

CLARINS - ROLL-ON DEODORANT ALUMINUM CHLOROHYDRATE - ANTIPERSPIRANT, LONG-LASTING, ALCOHOL-FREE 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58668-5971
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	140 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ROSEMARY (UNII: IJ67X351P9)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
AGATHOSMA BETULINA LEAF (UNII: 369DDH39Z0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58668-5971-1	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	02/01/2021

Labeler - Laboratoires Clarins (266317555)