Label: ANTIPERSPIRANT ODABAN- spray antiperspirant odaban spray
- NDC Code(s): 84788-0001-1
- Packager: Ryma-Pharm GmbH
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 27, 2024
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- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- ACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
Drug Facts Active Ingredient Aluminium Chloride 14,5% ODABAN® Antiperspirant Spray is a safe and simple antiperspirant that protects against excessive sweating and odour. Up to 90% sweat reduction after only 3 applications. Caution: Do not spray in eyes or apply to irritated skin. Avoid contact with clothing. Made in Germany by: RYMA PHARM GmbH, An der Eiche 14, 34327 Körle, Germany Made for: Archifox GmbH & Co. KG, Im Kitzwinkel 2, 34327 Körle, Germany Filling height Inactive Ingredients Aqua, Pentylene Glycol, 1,2-Heptanediol Purpose Antiperspirant Questions Call +1 (646) 566-6506 Directions Apply at bedtime. Ensure skin is clean and dry. Use only one pump per armpit or body area. Uses Decreases excessive sweating Warnings For external use only Do not use on broken skin Stop use if rash or irritation occurs Ask a doctor before use if you have kidney disease Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center.
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INGREDIENTS AND APPEARANCE
ANTIPERSPIRANT ODABAN
spray antiperspirant odaban sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84788-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE 4.35 mg in 30 mL Inactive Ingredients Ingredient Name Strength AQUA REGIA (UNII: X3TT5X989E) PENTYLENE GLYCOL (UNII: 50C1307PZG) (6R)-2-METHYL-6-((1R,3AS,4E,7AR)-OCTAHYDRO-4-((2Z)-2-((5S)-5-HYDROXY-2-METHYLENECYCLOHEXYLIDENE)ETHYLIDENE)-7A-METHYL-1H-INDEN-1-YL)-2,4-HEPTANEDIOL (UNII: UH3E0E5N53) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84788-0001-1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2024 Labeler - Ryma-Pharm GmbH (341264040) Registrant - Ryma-Pharm GmbH (341264040) Establishment Name Address ID/FEI Business Operations Ryma-Pharm GmbH 341264040 manufacture(84788-0001)