Label: PEACE OUT ACNE SERUM- salicylic acid lotion
- NDC Code(s): 71494-102-30
- Packager: Peace Out LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 3, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
- Uses
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Warnings
For external use only.
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Directions
For products applied to and left on the skin:
- 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
- Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.
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Inactive Ingredients
Water (AQUA/EAU), Propanediol, Dimethicone, Sodium Polyacryloyldimethyl Taurate, Niacinamide, Isopentyldiol, Zinc PCA, Potassium Azeloyl Diglycinate, Butylene Glycol, Ethylhexyl Olivate, Polysilicone-11, Potassium Hydroxide, 3-0-Ethyl Ascorbic Acid, Decyl Glucoside, Sodium Acrylates Copolymer, Polyglyceryl-4 Oleate, Tocopheryl Acetate, Glycerin, Caprylyl Glycol, Disodium EDTA, Gentelia Asiatica Extract, Lavandula Hybrida Grosso Herb Oil, Trifolium Pratense (Clover) Flower Extract, Ethylhexylglycerin, Aloe Barbadensis Leaf Extract, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, 1,2-Hexanediol, Sodium Hyaluronate, Phenoxyethanol, Saccharide Isomerate, Maltodextrin, Ethoxydiglycol, Totarol
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INGREDIENTS AND APPEARANCE
PEACE OUT ACNE SERUM
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71494-102 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 WATER (UNII: 059QF0KO0R) PROPANEDIOL (UNII: 5965N8W85T) DIMETHICONE (UNII: 92RU3N3Y1O) NIACINAMIDE (UNII: 25X51I8RD4) ISOPENTYLDIOL (UNII: 19NOL5474Q) SODIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: NG5NG5733T) ZINC PIDOLATE (UNII: C32PQ86DH4) POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP) ETHYLHEXYL OLIVATE (UNII: HTC7G3S2PV) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U) LAVANDIN OIL (UNII: 9RES347CKG) TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALOE VERA LEAF (UNII: ZY81Z83H0X) BERGAMOT OIL (UNII: 39W1PKE3JI) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PHENOXYETHANOL (UNII: HIE492ZZ3T) SACCHARIDE ISOMERATE (UNII: W8K377W98I) MALTODEXTRIN (UNII: 7CVR7L4A2D) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) TOTAROL (UNII: 67NH2854WW) POLYGLYCERYL-4 OLEATE (UNII: 15B05TY4GX) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71494-102-30 1 in 1 CARTON 05/06/2020 1 30 mL 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 05/06/2020 Labeler - Peace Out LLC. (043143413)
