Label: MDP HYALURONIC ACID UV CLEAR SUNSCREEN SPF 55- zinc oxide, homosalate, octocrylene, octisalate cream
- NDC Code(s): 72220-001-01
- Packager: SKINIDEA CO., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 30, 2024
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- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
- For sunscreen use:
- apply liberally 15 minutes before sun exposure
- use a water resistant sunscreen if swimming or sweating
- reapply at least every 2 hours
Sun Protection Measures.
Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and othersun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeve shirts, pants, hats, and sunglasses
- children under 6 months: Ask a doctor
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Inactive ingredients:
Water, Caprylic/Capric Triglyceride, Propanediol, Glycerin, Coco-Caprylate/Caprate, Cetearyl Olivate, 1,2-Hexanediol, Pentylene Glycol, Sorbitan Olivate, Cetearyl Alcohol, Glyceryl Stearate, Potassium Cetyl Phosphate, Lauroyl Lysine, Polyhydroxystearic Acid, Hydroxyacetophenone, Panthenol, Sodium Polyacryloyldimethyl Taurate, Triethoxycaprylylsilane, Acrylates Copolymer, Stearic Acid, Tromethamine, Sphingomonas Ferment Extract, Neopentyl Glycol Diethylhexanoate, Polyacrylate Crosspolymer-6, Hydroxy propyl Methylcellulose Stearoxy Ether, Trisodium Ethylenediamine Disuccinate, Citrullus Lanatus (Watermelon) Fruit Extract, Citric Acid, Acetyl Glucosamine, Sodium Hyaluronate, Biosaccharide Gum-1, Ethylhexylglycerin, Sodium Hyaluronate Crosspolymer, Gluconolactone, Salix Alba (Willow) Bark Extract, Butylene Glycol, Hydrogenated Lecithin, Caprylyl Glycol, Fragaria Vesca (Strawberry) Fruit Extract, Malus Domestica Fruit Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Ceramide NP, Punica Granatum Fruit Extract, Cholesterol, Hydroxypropyltrimonium Hyaluronate, Phytosphingosine, Ceramide NG, Ceramide NS, Ceramide AP, Ceramide AS, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Potassium Hyaluronate, Ceramide EOP, Fragrance
- Other information
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- Package Labeling:
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INGREDIENTS AND APPEARANCE
MDP HYALURONIC ACID UV CLEAR SUNSCREEN SPF 55
zinc oxide, homosalate, octocrylene, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72220-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 103.8 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 60 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PROPANEDIOL (UNII: 5965N8W85T) GLYCERIN (UNII: PDC6A3C0OX) COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H) CETEARYL OLIVATE (UNII: 58B69Q84JO) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) PENTYLENE GLYCOL (UNII: 50C1307PZG) SORBITAN OLIVATE (UNII: MDL271E3GR) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) LAUROYL LYSINE (UNII: 113171Q70B) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) PANTHENOL (UNII: WV9CM0O67Z) SODIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: NG5NG5733T) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) STEARIC ACID (UNII: 4ELV7Z65AP) TROMETHAMINE (UNII: 023C2WHX2V) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) WATERMELON (UNII: 231473QB6R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) N-ACETYLGLUCOSAMINE (UNII: V956696549) HYALURONATE SODIUM (UNII: YSE9PPT4TH) BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLUCONOLACTONE (UNII: WQ29KQ9POT) SALIX ALBA BARK (UNII: 205MXS71H7) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLYL GLYCOL (UNII: 00YIU5438U) FRAGARIA VESCA FRUIT (UNII: CG6IX3GCMU) APPLE (UNII: B423VGH5S9) CRANBERRY (UNII: 0MVO31Q3QS) CERAMIDE NP (UNII: 4370DF050B) POMEGRANATE (UNII: 56687D1Z4D) CHOLESTEROL (UNII: 97C5T2UQ7J) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) CERAMIDE NG (UNII: C04977SRJ5) CERAMIDE NS (UNII: V7M2259XJM) CERAMIDE AP (UNII: F1X8L2B00J) SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93) HYALURONIC ACID (UNII: S270N0TRQY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72220-001-01 1 in 1 CARTON 08/01/2024 1 40 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/01/2024 Labeler - SKINIDEA CO., LTD (690416325) Establishment Name Address ID/FEI Business Operations Cosmax, Inc. 689049693 manufacture(72220-001)
