Label: AQUAX REPELLENT- ethyl butylacetylaminopropionate cream
- NDC Code(s): 82160-252-01
- Packager: Pella Pharmaceuticals Co. Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 25, 2021
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- Forms and presentation
- Active Ingredient
- Inactive Ingredients
- Purpose
- Properties
- Indications
- Precautions
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Warnings
- For external use only.
- Do not apply to eyes or mouth, and apply sparingly around ears.
- Do not allow use by small children without adult supervision.
- Never use repellent over cuts, wounds or irritated skin.
- If you are allergic to any of the ingredients listed, you should check with your doctor or pharmacist before you use the product
- Contraindications
- Side effects
- Dosage and administration
- Storage conditions
- Primary Package
- Secondary Package
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INGREDIENTS AND APPEARANCE
AQUAX REPELLENT
ethyl butylacetylaminopropionate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82160-252 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ETHYL BUTYLACETYLAMINOPROPIONATE (UNII: 65GQA237EH) (ETHYL BUTYLACETYLAMINOPROPIONATE - UNII:65GQA237EH) ETHYL BUTYLACETYLAMINOPROPIONATE 75 mg in 75 g Inactive Ingredients Ingredient Name Strength MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PROPYLPARABEN (UNII: Z8IX2SC1OH) SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW) SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) WATER (UNII: 059QF0KO0R) POLYSORBATE 80 (UNII: 6OZP39ZG8H) BIS-PEG/PPG-16/16 PEG/PPG-16/16 DIMETHICONE (UNII: 55A74AJ3KB) BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) CETEARETH-25 (UNII: 8FA93U5T67) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARETH-22 (UNII: 28VZG1E234) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82160-252-01 1 in 1 CARTON 10/04/2010 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 unapproved drug other 10/04/2010 Labeler - Pella Pharmaceuticals Co. Ltd (562370925)