HCS ROLL-ON ANTIPERSPIRANT- aluminum chlorohydrate liquid

HCS Roll-on Antiperspirant by

Drug Labeling and Warnings

HCS Roll-on Antiperspirant by is a Otc medication manufactured, distributed, or labeled by Concordance Healthcare Solutions, LLC., Ken Prima Cosmeceuticals SDN BHD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Aluminum Chlorohydrate 4.5%

Purpose

Antiperspirant

Use

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.

Keep out of reach of children. If accidently swallowed, get medical help or contact Poison Control Center right away.

Directions

Apply to underarms only.

Inactive ingredients

Butylated Hydroxytoluene, Cetylstearyl Alcohol, Diazolidinyl Urea, Dimethicone, Disodium EDTA, Fragrance, Glycerin, Glyceryl stearate, Hydroxyethylcellulose, Methylparaben, Mineral Oil, Propylparaben, Sorbitan Monostearate. Stearic acid, Triethytamine, Tween-60, Water

Principal Display Panel – 1 Bottle

HCS

NDC: 83506-004-01

Clean Fresh Scent
Roll-On
Antiperspirant/
Deodorant

• Fights Wetness & Odor

1.5 FL. OZ. (44ml)

INGREDIENTS AND APPEARANCE

HCS ROLL-ON ANTIPERSPIRANT 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83506-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Aluminum Chlorohydrate (UNII: HPN8MZW13M) (Aluminum Chlorohydrate - UNII:HPN8MZW13M)	Aluminum Chlorohydrate	45 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
Diazolidinyl Urea (UNII: H5RIZ3MPW4)
Dimethicone (UNII: 92RU3N3Y1O)
Edetate Calcium Disodium (UNII: 25IH6R4SGF)
Fragrance Clean ORC0600327 (UNII: 329LCV5BTF)
Glycerin (UNII: PDC6A3C0OX)
Glyceryl 1-Stearate (UNII: 258491E1RZ)
Hydroxyethyl Cellulose, Unspecified (UNII: T4V6TWG28D)
Methylparaben (UNII: A2I8C7HI9T)
Mineral Oil (UNII: T5L8T28FGP)
Propylparaben (UNII: Z8IX2SC1OH)
Sorbitan Monostearate (UNII: NVZ4I0H58X)
Stearic Acid (UNII: 4ELV7Z65AP)
Triethylamine (UNII: VOU728O6AY)
Polysorbate 60 (UNII: CAL22UVI4M)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83506-004-01	44 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/06/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	MO19	06/06/2023

Labeler - Concordance Healthcare Solutions, LLC. (080220245)

Establishment
Name	Address	ID/FEI	Business Operations
WUHAN ZONSEN MEDICAL PRODUCTS CO.,LTD		554474517	MANUFACTURE(83506-004)