Label: THINK EVERY DAY FACE SUNSCREEN SPF 30- zinc oxide lotion
- NDC Code(s): 60781-1011-1
- Packager: thinkOperations,LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 22, 2020
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
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Uses
Helps prevent sunburns if used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun
- Warning
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Directions
- apply liberally 15 minutes before sun exposure
- reapply
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every two hours
Sun Protection Measures: spending time in the sun increases your risk of skin cancer and early skin aging. To decreae this risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 am - 2 pm
- wear long-sleeved shirts, pants, hats and sunglasses
For children under 6 months: Ask a doctor
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INACTIVE INGREDIENT
Inactive ingredients Purified water, caprylic/capric triglyceride, polyglycery-4 isosterate, cetyl dimethicone, hexyl laurate, glycerin, hydrogenated methyl abietate (pine wood resin), iron oxide, magnesium sulfate, caprylhdroxamic acid, glyceryl caprylate, sorbitan sesquioleate, ribes rubrum (currant) fruit, helianthus annuus (sunflower) oil, simmondsia chineses (jojoba) seed oil, tocopherol, olea europaea (olive) fruit oil, hyalurounic acid (plant based), citrus paradisi (grapefruit)
- Other information
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
THINK EVERY DAY FACE SUNSCREEN SPF 30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60781-1011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 200 mg in 1 mL Inactive Ingredients Ingredient Name Strength CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) RIBES RUBRUM WHOLE (UNII: F5C4R60S7W) FERRIC OXIDE RED (UNII: 1K09F3G675) GRAPEFRUIT (UNII: O82C39RR8C) TRICAPRIN (UNII: O1PB8EU98M) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) JOJOBA OIL (UNII: 724GKU717M) HYALURONIC ACID (UNII: S270N0TRQY) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) SUNFLOWER OIL (UNII: 3W1JG795YI) TOCOPHEROL (UNII: R0ZB2556P8) OLIVE OIL (UNII: 6UYK2W1W1E) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) HEXYL LAURATE (UNII: 4CG9F9W01Q) HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O) TRICAPRILIN (UNII: 6P92858988) WATER (UNII: 059QF0KO0R) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) GLYCERIN (UNII: PDC6A3C0OX) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60781-1011-1 59 mL in 1 TUBE; Type 0: Not a Combination Product 09/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M020 09/21/2020 Labeler - thinkOperations,LLC (808883636) Registrant - Topiderm, Inc. (049121643) Establishment Name Address ID/FEI Business Operations Topiderm, Inc. 049121643 MANUFACTURE(60781-1011)
