Label: UV CLEAR DEEP TINT- octinoxate, zinc oxide sunscreen lotion
- NDC Code(s): 72043-2530-1, 72043-2530-2
- Packager: CP Skin Health Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 8, 2024
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- Official Label (Printer Friendly)
- Warnings
- Keep out of reach of children
- Uses
- Uses
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Directions
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 other sun protection measures including: limit time in the sun, especially from 10 am to 2 pm. Wear long-sleeve shirts, pants, hats, and sunglasses. Children under 6 months: ask a physician.
- Active Ingredients
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Inactive Ingredients
water, cyclopentasiloxane, niacinamide, octyldodecyln eopentanoate, hydroxyethyl acrylate/sodium acryloldimethyl taurate copolymer, butylee glycol, isopropyl palmitate, phenoxyethanol, polyisobutene, ethylheyl stearate, triethoxycaprylylsilane, tocopheryl acetate, PEG-7 trimethylolpropane coconut ether, oleth-3 phosphate, iodopropynyl butylcarbamate, latic acid, sodiym hyaluroate, iron oxides
- Questions
- Labeling
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INGREDIENTS AND APPEARANCE
UV CLEAR DEEP TINT
octinoxate, zinc oxide sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72043-2530 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 750 g in 1000 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 900 g in 1000 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) LACTIC ACID (UNII: 33X04XA5AT) HYALURONIC ACID (UNII: S270N0TRQY) NIACINAMIDE (UNII: 25X51I8RD4) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) PHOSPHORIC ACID (UNII: E4GA8884NN) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) PEG-7 TRIMETHYLOLPROPANE COCONUT ETHER (UNII: MVJ3AD73GG) Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72043-2530-1 50 g in 1 BOTTLE; Type 0: Not a Combination Product 05/08/2024 2 NDC:72043-2530-2 2 g in 1 PACKET; Type 0: Not a Combination Product 05/08/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/08/2024 Labeler - CP Skin Health Group, Inc. (611921669) Registrant - Swiss-American CDMO, LLC (080170933) Establishment Name Address ID/FEI Business Operations Swiss-American CDMO, LLC 080170933 manufacture(72043-2530)
