ANTI-PERSPIRANT DEODORANT ROLL-ON UNSCENTED- aluminum chlorohydrate liquid

Anti-Perspirant Deodorant Roll-On by

Drug Labeling and Warnings

Anti-Perspirant Deodorant Roll-On by is a Otc medication manufactured, distributed, or labeled by Hydrox Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Aluminum Chlorohydrate, 10% - Anhydrous Basis

Purpose

Antiperspirant

Use

Reduces underarm wetness.

Warnings

FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF CHILDREN.

Do not use on broken skin.

Stop use if rash or irritation occurs.

Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

Directions

Apply to underarms. Use daily for best results.

Inactive ingredients

Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Tetrasodium EDTA

PRINCIPAL DISPLAY PANEL 

Personal Care

FreshMoment

Anti-Perspirant

Deocorant Roll-On

Alcohol Free

Helps Reduce Wetness

Fragrance Free

Dye Free Formula

Made in USA

INGREDIENTS AND APPEARANCE

ANTI-PERSPIRANT DEODORANT ROLL-ON   UNSCENTED
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10565-074
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Aluminum Chlorohydrate (UNII: HPN8MZW13M) (Aluminum Chlorohydrate - UNII:HPN8MZW13M)	Aluminum Chlorohydrate	10 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
Glycerin (UNII: PDC6A3C0OX)
Polysorbate 20 (UNII: 7T1F30V5YH)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10565-074-01	45 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	03/20/2012
2	NDC: 10565-074-02	59 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	03/20/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part350	03/20/2012

Labeler - Hydrox Laboratories (025164302)

Registrant - Hydrox Laboratories (025164302)

Establishment
Name	Address	ID/FEI	Business Operations
Hydrox Laboratories		025164302	label(10565-074) , manufacture(10565-074) , pack(10565-074)