Label: SPF30 SUNSCREEN CARIPOSA- titanium dioxide, zinc oxide spray
- NDC Code(s): 84267-003-02
- 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 ingredients Purpose
- 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 reach of children. If swallowed,get medical help orcontact a Poison Control Center right away
-
Directions:
- apply liberally 15 minutes before sun exposure and as needed. Reapply:
- after 80 minutes of sweeming or sweating
- immidiately after towel drying
- at least every 2 hours
- Sun Protection Measures. Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk. regularly usea sunscreen wrtha Broad Spectrum SPF value of15 or higher and other suncrin protection measures including:
- limrt time in the sun, especial from 10a.m. -2 p.rn.•wear long-sleeve shorts , pants, hats and sunglasses
- children under 6 months of age: ask a doctor
- Other information
-
Inactive ingredients
ALOE
ALUMINA
ALUMINUM STARCH OCTENYLSUCCINATE
ALKYL (C12-15) BENZOATE
CAMELLIA SINENSIS FLOWER EXTRACT
CETYL PEG/PPG-10/1 DIMETHICONE
CUCUMIS SATIVUS FRUET EXTRACT
DIMETHICONE
EDETATE DISODIUM
ETHYLHEXYL PALMITATE
ETHYLHEXYLGLYCERIN
GLYCERIN
HYDROGEN DIMETHICONE
MENTHA PIPERITA (UNII: 79M2M2UDA9)
RICE BRAN, DEFATTED
PHENOXYETHANOL
PROPANEDIOL
POMEGRANATE JUICE
ROSMARINUS OFFICINALIS LEAF EXTRACT
SILICON DIOXIDE
SODIUM CHLORIDE
SORBITAN OLIVATE
STYRENE/ACRYLAMIDE COPOLYMER
GRAPE SEED EXTRACT
WATER - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SPF30 SUNSCREEN CARIPOSA
titanium dioxide, zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84267-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 4.5 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 4 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) ALUMINUM OXIDE (UNII: LMI26O6933) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) CUCUMIS SATIVUS LEAF (UNII: Q6S42514LP) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYL PALMITATE (UNII: 2865993309) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI) MENTHA PIPERITA (UNII: 79M2M2UDA9) RICE BRAN, DEFATTED (UNII: H6597RO5A2) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPANEDIOL (UNII: 5965N8W85T) POMEGRANATE JUICE (UNII: 99S671U9KB) ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM CHLORIDE (UNII: 451W47IQ8X) SORBITAN OLIVATE (UNII: MDL271E3GR) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) GRAPE (UNII: 6X543N684K) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84267-003-02 99 g in 1 CONTAINER; Type 0: Not a Combination Product 04/18/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/18/2024 Labeler - Talent Brands Company LLC (061158156) Registrant - Bridgeview Investments LLC (035014854) Establishment Name Address ID/FEI Business Operations DermaCare researcg Labs, LLC 116817470 manufacture(84267-003)
