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 Ingredients:

AQUA/WATER/EAU. DIPROPYLENE GLYCOL. PEG-40 HYDROGENATED CASTOR OIL. METHYL GLUCETH-20. POLYSORBATE 20. HYDROXYETHYLCELLULOSE. PARFUM/FRAGRANCE. PROPANEDIOL. GLYCERIN. BENZYL ALCOHOL. HYDROXYACETOPHENONE. PHENOXYETHANOL. DISODIUM EDTA. CHONDRUS CRISPUS EXTRACT. HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT. [C0493E]

Questions or comments?

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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: 58668-5981
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)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
PROPANEDIOL (UNII: 5965N8W85T)
GLYCERIN (UNII: PDC6A3C0OX)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58668-5981-1	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M	10/01/2024

Labeler - Laboratoires Clarins (266317555)