Label: DIFFERIN ACNE CLEARING BODY SCRUB- salicylic acid liquid
- NDC Code(s): 0299-4609-00, 0299-4609-05
- Packager: Galderma Laboratories, L.P.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
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Inactive Ingredients
Acrylates Copolymer, Aloe Barbadensis Leaf Extract, Butylene Glycol, Butyrospermum Parkii (Shea) Butter, Caprylic/Capric Triglyceride, Cocamidopropyl Betaine, Coco-Betaine, Coconut Acids, Disodium EDTA, Fragrance, Glycerin, Glycol Distearate, Glycolic Acid, Hydroxypropyl Methylcellulose Kaolin, Laureth-4, Lauroyl/Myristoyl Methyl Glucamide, Mannitol, Microcrystalline Cellulose, Olive Oil Peg-8 Esters, Paraffin, Polyquaternium-39, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Retinyl Palmitate, Salicylic Acid, Silica, Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Sodium Hydroxide, Sodium Sulfate, Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate, Ultramarines, Water
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- PRINCIPAL DISPLAY PANEL - 8 FL OZ tube
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INGREDIENTS AND APPEARANCE
DIFFERIN ACNE CLEARING BODY SCRUB
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0299-4609 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength Butyl Acrylate/Methyl Methacrylate/Methacrylic Acid Copolymer (18000 Mw) (UNII: JZ1374NL9E) Aloe Vera Leaf (UNII: ZY81Z83H0X) Butylene Glycol (UNII: 3XUS85K0RA) Shea Butter (UNII: K49155WL9Y) Medium-Chain Triglycerides (UNII: C9H2L21V7U) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Coco-Betaine (UNII: 03DH2IZ3FY) Coconut Acid (UNII: 40U37V505D) Edetate Disodium (UNII: 7FLD91C86K) Glycerin (UNII: PDC6A3C0OX) Glycol Distearate (UNII: 13W7MDN21W) Glycolic Acid (UNII: 0WT12SX38S) Hypromellose, Unspecified (UNII: 3NXW29V3WO) Kaolin (UNII: 24H4NWX5CO) Laureth-4 (UNII: 6HQ855798J) Lauroyl/Myristoyl Methyl Glucamide (UNII: SC667B999P) Mannitol (UNII: 3OWL53L36A) Microcrystalline Cellulose (UNII: OP1R32D61U) Paraffin (UNII: I9O0E3H2ZE) Polyquaternium-39 (22.5/51/26.5 Acrylic Acid/Acrylamide/Dadmac; 1600000 Mw) (UNII: X2NH1K9F8K) Almond Oil (UNII: 66YXD4DKO9) Vitamin A Palmitate (UNII: 1D1K0N0VVC) Silicon Dioxide (UNII: ETJ7Z6XBU4) Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U) Sodium Chloride (UNII: 451W47IQ8X) Sodium Hydroxide (UNII: 55X04QC32I) Sodium Sulfate (UNII: 0YPR65R21J) Cocoa Butter (UNII: 512OYT1CRR) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Ultramarine Blue (UNII: I39WR998BI) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0299-4609-00 237 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2021 2 NDC:0299-4609-05 15 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2021 Labeler - Galderma Laboratories, L.P. (047350186) Establishment Name Address ID/FEI Business Operations Cosmetic Essence, LLC dba Voyant Beauty 032565959 manufacture(0299-4609)