ANTI-PERSPIRANT DEODORANT- aluminium zirconium tetrachlorohydrex gly liquid

Anti-Perspirant Deodorant by

Drug Labeling and Warnings

Anti-Perspirant Deodorant by is a Otc medication manufactured, distributed, or labeled by Xtreme Tools International, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminium Zirconium Tetrachlorohydrex Gly (15%)

Purpose

Antiperspirant

Use

Reduces underarm wetness

Warnings

For external use only.

DO NOT USE

Do not use on broken skin.

STOP USE

Stop use and Ask Doctor if rash or irritation occurs.

ASK DOCTOR

​ Ask a doctor before use if you have kidney disease.

KEEP OUT OF REACH OF CHILDREN

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

Directions

Apply to underarms only.

Inactive Ingredients

Brassica Glycerides, Polyester-4, C 13-16 lsoparaffin, Heptyl Undecylenate, Cyclotetrasiloxane. Caprylic/Capric Triglyceride, PPG-14 Butyl Ether, Stearyl Alcohol, Fragrance

Questions or comments?

Call 1-305-622-7474 Monday through Friday 9:00 AM to 5:00 PM

Principal Display Panel

59 mL in Bottle; NDC: 74553-001-01

INGREDIENTS AND APPEARANCE

ANTI-PERSPIRANT DEODORANT 
aluminium zirconium tetrachlorohydrex gly liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74553-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE)	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 4 (UNII: CZ227117JE)
TRICAPRIN (UNII: O1PB8EU98M)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
POLYESTER (ADIPIC ACID, 1,6-HEXANEDIOL, NEOPENTYL GLYCOL) (UNII: 571593769G)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
C13-16 ISOPARAFFIN (UNII: LED42LZG6O)
BRASSICA JUNCEA SEED OIL (UNII: 4D13WHP5F7)
HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74553-001-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	10/06/2020

Labeler - Xtreme Tools International, Inc (125398904)

Registrant - Xtreme Tools International, Inc (125398904)

Establishment
Name	Address	ID/FEI	Business Operations
Xtreme Tools International, Inc		125398904	manufacture(74553-001)