Label: DERMA PELLA FACIAL CLEANSER FOR NORMAL SKIN- niacinamide solution
- NDC Code(s): 82160-757-01
- Packager: Pella Pharmaceuticals Co. Ltd
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated June 19, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Forms and Presentation
- Active Ingredients
-
Inactive Ingredients
Aqua, Glycerin, Cocamidopropyl Betain, Sodium C14-16 Olefin Sulfonate, Butylene Glycol, Polysorbate 20, Sodium Benzoate, Allantoin, Potassium Sorbate, Rosmarinus Officinalis (Rosemary) Leaf Extract, Disodium EDTA, Parfum, Citric Acid, Phenoxyethanol, 2-Bromo-2-Nitropropane-1,3-Diol, Tetrasodium EDTA, Benzoic Acid, Dehydroacetic Acid.
- Purpose
-
Properties
This foaming face wash penetrates deep into your pores, scrubbing them from the inside out to eliminate dirt and oils.
Rosemary Extract makes the skin feel soft and sparkling by purifying, soothing, hydrating and provides anti-aging properties to the skin because it enriched in zinc, and vitamins A, B6, and C.
Niacinamide (Vitamin B3) helps soothe and balance the appearance of skin tone.
Allantoin which is an effective moisturizing ingredient used for it is gentle and non-irritating qualities.
Paraben free, Alcohol free, SLS free, SLES free.
- Indications
- Precautions
- Warnings
- Contraindications
- Side Effects
- Dosage and Administration
- Storage Conditions
- Primary Package
-
INGREDIENTS AND APPEARANCE
DERMA PELLA FACIAL CLEANSER FOR NORMAL SKIN
niacinamide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82160-757 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SODIUM BENZOATE (UNII: OJ245FE5EU) ALLANTOIN (UNII: 344S277G0Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) BRONOPOL (UNII: 6PU1E16C9W) POLYSORBATE 20 (UNII: 7T1F30V5YH) BENZOIC ACID (UNII: 8SKN0B0MIM) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ROSEMARY (UNII: IJ67X351P9) WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) DEHYDROACETIC ACID (UNII: 2KAG279R6R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82160-757-01 150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/16/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/16/2023 Labeler - Pella Pharmaceuticals Co. Ltd (562370925)
