Label: SPF50 SUNSCREEN CARIPOSA- zinc oxide stick
- NDC Code(s): 84267-002-01
- Packager: Talent Brands Company LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 18, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings For external use only
- Do not use on
- When using this product
- Stop use and ask a doctor if
- Keep out of the reach of children
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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. 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 • children under 6 months of age: ask a doctor
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SPF50 SUNSCREEN CARIPOSA
zinc oxide stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84267-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 21.6 g in 100 g Inactive Ingredients Ingredient Name Strength ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) CERESIN (UNII: Q1LS2UJO3A) PARAFFIN (UNII: I9O0E3H2ZE) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SYNTHETIC WAX (1800 MW) (UNII: 248P1AUJ90) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84267-002-01 43 g in 1 CONTAINER; Type 0: Not a Combination Product 10/16/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/16/2023 Labeler - Talent Brands Company LLC (061158156) Registrant - Bridgeview Investments LLC (035014854) Establishment Name Address ID/FEI Business Operations DermaCare researcg Labs, LLC 116817470 manufacture(84267-002)