ANTIPERSPIRANT ANTISUDORIFIQUE spray

ANTIPERSPIRANT ANTISUDORIFIQUE by

Drug Labeling and Warnings

ANTIPERSPIRANT ANTISUDORIFIQUE by is a Otc medication manufactured, distributed, or labeled by Archifox GmbH & Co. KG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

DIRECTIONS Underarm use only.

WARNINGS

Decreases excessive sweating.

INACTIVE INGREDIENT

Dimethicone, Stearyl Alcohol, Kaolin, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Octyldodecanol, Tocopherol, BHT, Parfum.

INDICATIONS & USAGE

For external use only. Do not use on broken skin. Stop use if rash or irritation occurs. ‘Aska doctor before use if you have kidney disease. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center.

ACTIVE INGREDIENT

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

PURPOSE

PURPOSE: Antiperspirant

ACTIVE INGREDIENT

ACTIVE INGREDIENT: Aluminum Chloride 20%

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

ANTIPERSPIRANT ANTISUDORIFIQUE

odaban@ daily DISTRIBUTED BY: Archifox GmbH & Co. KG Im Kitzwinkel 2, 34327 Kérle, Germany www.odaban.com 025381 5 ANTIPERSPIRANT deo stick DRUG FACTS ACTIVE INGREDIEN’ PURPOSE: Aluminum Chloride 20%... Antiperspirant re Decreases excessive sweating. WARNINGS For external use only. Do not use on broken skin. Stop use if rash or irritation occurs. ‘Aska doctor before use if you have kidney disease. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center. DIRECTIONS Underarm use only. reat olan eS) Dimethicone, Stearyl Alcohol, Kaolin, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Octyldodecanol, Tocopherol, BHT, Parfum. QUESTIONS? Net Wt. 2.1 oz

INGREDIENTS AND APPEARANCE

ANTIPERSPIRANT ANTISUDORIFIQUE 
antiperspirant antisudorifique spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84724-0002(NDC:84788-0002)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	12.4 mg  in 62 mL

Inactive Ingredients
Ingredient Name	Strength
TOCOPHEROL (UNII: R0ZB2556P8)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
KAOLIN (UNII: 24H4NWX5CO)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
OCTYLDODECANOL (UNII: 461N1O614Y)
BHT (UNII: 1P9D0Z171K)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84724-0002-1	62 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/01/2025

Labeler - Archifox GmbH & Co. KG (315107452)

Registrant - Archifox GmbH & Co. KG (315107452)

Establishment
Name	Address	ID/FEI	Business Operations
Archifox GmbH & Co. KG		315107452	relabel(84724-0002)