Label: THRIVE DAILY DEFENSE SUNSCREEN BALM SPF30- zinc oxide cream
- NDC Code(s): 84138-0001-2
- 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, Polyglyceryl-4 Laurate/Sebacate, Polyglyceryl-6 Caprylate/Caprate, Undaria Pinnatifida (Wakame) Extract, Coffea Arabica (Coffee) Seed Oil, Polyhydroxystearic Acid, Cellulose Gum, Xanthan Gum, Phytic Acid, Fridericia Chica (Arrabidaea Chica) Extract, Lippia Alba Oil, Hamelia Patens Extract, Ethyl Macadamiate, Tasmannia Lanceolata Fruit/Leaf Extract, Helianthus Annuus (Sunflower) Seed Oil, Triethoxycaprylylsilane, Rosmarinus Officinalis (Rosemary) Leaf Extract, Caprylyl Glyceryl Ether, Caprylhydroxamic Acid, Fragrance.
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INGREDIENTS AND APPEARANCE
THRIVE DAILY DEFENSE SUNSCREEN BALM SPF30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84138-0001 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 COCO-CAPRYLATE (UNII: 4828G836N6) UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) LIPPIA ALBA TOP OIL (UNII: 34F635Y5Z2) HAMELIA PATENS LEAF (UNII: Y7N77A1XO2) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) XANTHAN GUM (UNII: TTV12P4NEE) 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) ARABICA COFFEE OIL (UNII: IK55HKE887) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84138-0001-2 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(84138-0001)
