Label: THINK ALOE AND TEA LEAVES ZINC OXIDE- zinc oxide lotion
- NDC Code(s): 60781-4698-1
- Packager: thinkOperations,LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 2, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- 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
- Warnings
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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 2 hours when exposed to sun
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 value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m
- wear long-sleeved shirts, pants, hats, and sunglasses
For children under 6 months: Ask a doctor
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Inactive ingredients
Purified Water, Caprylic/Capric Triglyceride, Polyglyceryl-4 Isostearate, Glycerin, Hydrogenated Glyceryl Abietate, Hexyl Laurate, Cetyl Dimethicone, Sorbitan Sesquioleate, Magnesium Sulfate, Tocopherol, Sodium Hyaluronate, Helianthus Annuus (Sunflower) Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Olea Europaea (Olive) Fruit Oil, Citrus Paradisi (Grapefruit) Peel Oil, Aloe Barbadensis Leaf Juice, Hydrogenated Castor Oil, Triethoxycaprylylsilane, Caprylhydroxamic Acid, Glyceryl Caprylate, Natural Fragrance Oil.
- Other information
- For Questions
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 89 ml Tube Label
-
INGREDIENTS AND APPEARANCE
THINK ALOE AND TEA LEAVES ZINC OXIDE
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60781-4698 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 WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) GLYCERIN (UNII: PDC6A3C0OX) HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O) CETYL DIMETHICONE 150 (UNII: 5L694Y0T22) HEXYL LAURATE (UNII: 4CG9F9W01Q) DIMETHICONE (UNII: 92RU3N3Y1O) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) SUNFLOWER OIL (UNII: 3W1JG795YI) JOJOBA OIL (UNII: 724GKU717M) OLIVE OIL (UNII: 6UYK2W1W1E) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60781-4698-1 89 mL in 1 TUBE; Type 0: Not a Combination Product 07/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M020 07/02/2022 Labeler - thinkOperations,LLC (808883636) Registrant - Topiderm, Inc. (049121643) Establishment Name Address ID/FEI Business Operations Topiderm, Inc. 049121643 MANUFACTURE(60781-4698) Establishment Name Address ID/FEI Business Operations Topix Pharmaceuticals, Inc. 117745066 PACK(60781-4698)