ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate spray

Anti-Perspirant Deodorant by

Drug Labeling and Warnings

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

Drug Details [pdf]

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Drug Facts

Active ingredient

Aluminum Chlorohydrate, 13% - 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

Hold two inches from underarm and spray. Use daily for best results.

Inactive ingredients

Purified Water, Isopropyl Alcohol, Propylene Glycol, Peg-40 Hydrogenated Castor Oil, Fragrance.

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MFG BY:
HYDROX LABORATORIES
825 Tollgate Rd. Elgin, IL 60123

PRINCIPAL DISPLAY PANEL

Personal Care

FreshMoment

Anti-Perspirant
Deodorant Spray

Helps Reduce Wetness
Spring Fresh Fragrance

MADE IN USA

2 FL. OZ. (59mL)

INGREDIENTS AND APPEARANCE

ANTI-PERSPIRANT DEODORANT 
aluminum chlorohydrate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10565-067
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isopropyl Alcohol (UNII: ND2M416302)
Propylene Glycol (UNII: 6DC9Q167V3)
Polyoxyl 40 Hydrogenated Castor Oil (UNII: 7YC686GQ8F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10565-067-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/11/2011
2	NDC: 10565-067-04	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/11/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	11/11/2011

Labeler - Hydrox Laboratories (025164302)

Registrant - Hydrox Laboratories (025164302)

Establishment
Name	Address	ID/FEI	Business Operations
Hydrox Laboratories		025164302	MANUFACTURE(10565-067) , label(10565-067) , pack(10565-067)