ROLL ON ANTI PERSPIRANT ALCOHOL FREE- aluminum chlorohydrate solution

Roll On Anti Perspirant by

Drug Labeling and Warnings

Roll On Anti Perspirant 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, Fragrance, Tetrasodium EDTA

PRINCIPAL DISPLAY PANEL 

Personal Care

FreshMoment

Anti-Perspirant
Deodorant Roll-On
Alcohol-Free

Helps Reduce Wetness
Spring Fresh Fragrance

MADE IN USA

1.5 FL. OZ. (45mL)

INGREDIENTS AND APPEARANCE

ROLL ON ANTI PERSPIRANT  ALCOHOL FREE
aluminum chlorohydrate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10565-066
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: 10565-066-02	45 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	10/26/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part350	10/26/2011

Labeler - Hydrox Laboratories (025164302)

Registrant - Hydrox Laboratories (025164302)

Establishment
Name	Address	ID/FEI	Business Operations
Hydrox Laboratories		025164302	MANUFACTURE(10565-066) , label(10565-066) , pack(10565-066)