Label: AQUAX DEO- aluminum chlorohydrate cream
- NDC Code(s): 82160-313-01
- Packager: Pella Pharmaceuticals Co. Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 25, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Forms and presentation
- Active Ingredient
- Inactive Ingredients
- Purpose
- Properties
- Indications
- Precautions
- Warnings
- Contraindications
- Side effects
- Dosage and administration
- Storage conditions
- Primary Package
- Secondary Package
-
INGREDIENTS AND APPEARANCE
AQUAX DEO
aluminum chlorohydrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82160-313 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 150 mg in 75 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) CETEARETH-22 (UNII: 28VZG1E234) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PETROLATUM (UNII: 4T6H12BN9U) CETEARETH-25 (UNII: 8FA93U5T67) SODIUM CITRATE (UNII: 1Q73Q2JULR) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82160-313-01 1 in 1 CARTON 03/15/2011 1 75 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 03/15/2011 Labeler - Pella Pharmaceuticals Co. Ltd (562370925)