Label: NATURIUM ENCAPSULATED SALICYLIC ACID MOISTURIZER 0.75%- salicylic acid lotion
- NDC Code(s): 76354-121-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 16, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only.
When using this product
- skin irritation and dryness are more likely to occur when using another topical acne product at the same time. If irritation occurs, use only one acne product at a time.
- Avoid eye area. In case of eye contact, flush gently and thoroughly with water. Do not apply to broken or irritated skin.
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Directions
- clean the skin thoroughly before applying this product.
- cover the entire affected area with a thin layer one to three times daily.
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
- if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use and ask a doctor.
- Other Information
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Inactive Ingredients
Aqua (Water), Propanediol, Butylene Glycol, Octyldodecanol, Dimethicone, Glyceryl Stearate, Coco-Caprylate/Caprate, Glycerin, Cetearyl Alcohol, Triheptanoin, Octadecenedioic Acid, Silybum Marianum Extract, Magnesium PCA, Amylopectin, Niacinamide, Succinoglycan, Bisabolol, Nelumbo Nucifera Flower Water, Nymphaea Caerulea Flower Water, Palmitic Acid, Lecithin, Physalis Angulata Extract, Acetyl Glucosamine, Castor Oil/IPDI Copolymer, Caprylic/Capric Triglyceride, Dilinoleic Acid/Butanediol Copolymer, Carbomer, C9-12 Alkane, Behenyl Alcohol, Stearic Acid, Dipropylene Glycol, Polysorbate 20, Dextrin, Polydextrose, Caprylyl Glycol, 1,2-Hexanediol, Cetyl Alcohol, Lauryl Alcohol, Myristyl Alcohol, Sodium Hydroxide, Phenoxyethanol, Tocopherol.
- Product Packaging
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INGREDIENTS AND APPEARANCE
NATURIUM ENCAPSULATED SALICYLIC ACID MOISTURIZER 0.75%
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-121 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 7.5 mg in 1 g Inactive Ingredients Ingredient Name Strength NIACINAMIDE (UNII: 25X51I8RD4) C9-12 ALKANE (UNII: 7J5R5W72QM) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) TRIHEPTANOIN (UNII: 2P6O7CFW5K) OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG) MILK THISTLE (UNII: U946SH95EE) MAGNESIUM PIDOLATE (UNII: V5PC588N7G) WATER (UNII: 059QF0KO0R) AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777) PROPANEDIOL (UNII: 5965N8W85T) GLYCERIN (UNII: PDC6A3C0OX) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PALMITIC ACID (UNII: 2V16EO95H1) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ICODEXTRIN (UNII: 2NX48Z0A9G) POLYDEXTROSE (UNII: VH2XOU12IE) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETYL ALCOHOL (UNII: 936JST6JCN) MYRISTYL ALCOHOL (UNII: V42034O9PU) PHENOXYETHANOL (UNII: HIE492ZZ3T) TOCOPHEROL (UNII: R0ZB2556P8) OCTYLDODECANOL (UNII: 461N1O614Y) LAURYL ALCOHOL (UNII: 178A96NLP2) DIMETHICONE (UNII: 92RU3N3Y1O) LEVOMENOL (UNII: 24WE03BX2T) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYSORBATE 20 (UNII: 7T1F30V5YH) NYMPHAEA CAERULEA FLOWER VOLATILE OIL (UNII: 869334Z0JF) N-ACETYLGLUCOSAMINE (UNII: V956696549) STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM HYDROXIDE (UNII: 55X04QC32I) NELUMBO NUCIFERA FLOWER OIL (UNII: P658Q19EG2) PHYSALIS ANGULATA WHOLE (UNII: W4TKW9D5GG) DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O) DOCOSANOL (UNII: 9G1OE216XY) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) DIPROPYLENE GLYCOL (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-121-01 1 in 1 CARTON 06/17/2022 1 50 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/17/2022 Labeler - e.l.f. Cosmetics, Inc (093902816)
