Label: THRIVE DAILY SUNSCREEN FOR SENSITIVE SKIN SPF 30- zinc oxide cream
- NDC Code(s): 84138-0002-2
- Packager: Thrive Natural Care, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 1, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
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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 value of 15 SPF 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
Children under 6 months of age: ask a doctor
- Other information
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Inactive ingredients
Water, Coco-Caprylate, Dicaprylyl Carbonate, Glycerin, Microcrystalline Cellulose, Lauryl Glucoside, Propanediol, Cetyl Alcohol, Polyglyceryl-2 Dipolyhydroxystearate, Ethyl Macadamiate, Polyhydroxystearic Acid, Saccharide Isomerate, Fridericia Chica (Arrabidaea Chica) Extract, Hamelia Patens Extract, Xanthan Gum, Cellulose Gum, Tasmannia Lanceolata Fruit/Leaf Extract, Polyglyceryl-4 Laurate/Sebacate, Polyglyceryl-6 Caprylate/Caprate, Undaria Pinnatifida (Wakame) Extract, Phytic Acid, Helianthus Annuus (Sunflower) Seed Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Triethoxycaprylylsilane, Caprylyl Glyceryl Ether, Caprylhydroxamic Acid.
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INGREDIENTS AND APPEARANCE
THRIVE DAILY SUNSCREEN FOR SENSITIVE SKIN SPF 30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84138-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 20 g in 100 mL Inactive Ingredients Ingredient Name Strength SACCHARIDE ISOMERATE (UNII: W8K377W98I) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) XANTHAN GUM (UNII: TTV12P4NEE) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) HAMELIA PATENS LEAF (UNII: Y7N77A1XO2) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) PROPANEDIOL (UNII: 5965N8W85T) ETHYL MACADAMIATE (UNII: ANA2NCS6V1) TASMANNIA LANCEOLATA FRUIT (UNII: PNT2HDL13Q) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) GLYCERIN (UNII: PDC6A3C0OX) FYTIC ACID (UNII: 7IGF0S7R8I) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) POLYGLYCERYL-4 LAURATE (UNII: 82V7NG3DYT) ROSEMARY (UNII: IJ67X351P9) CAPRYLYL GLYCERYL ETHER (UNII: MI97BW74XZ) SUNFLOWER OIL (UNII: 3W1JG795YI) POLYGLYCERYL-6 CAPRYLATE (UNII: DGV8R54VG7) FRIDERICIA CHICA LEAF (UNII: N0KHT56R6P) CETYL ALCOHOL (UNII: 936JST6JCN) WATER (UNII: 059QF0KO0R) COCO-CAPRYLATE (UNII: 4828G836N6) UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84138-0002-2 1 in 1 CARTON 03/01/2024 1 60 mL in 1 BOTTLE, PLASTIC; 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 03/01/2024 Labeler - Thrive Natural Care, Inc (066150506) Establishment Name Address ID/FEI Business Operations Columbia Cosmetics Manufacturing, Inc 068267863 manufacture(84138-0002)
