Label: SOLAIRE PEAU PARFAITE MINERAL SCREEN SPF 30- zinc oxide cream
- NDC Code(s): 63505-771-00
- Packager: Yves Rocher North America Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 2024
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- Drug Facts
- Active Ingredients
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• Apply generously and evenly 15 minutes before sun exposure. • reapply: • after 40 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 am - 2 pm • wear long-sleeved shirts, pants, hats, and sunglasses. • For use on children less than 6 months of age, consult a doctor
- Other Information
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Inactive Ingredients
Water, Coco-Caprylate, Caprylic/ Capric Triglyceride, Cetearyl Isononanoate, Ethylhexyl Palmitate, Glycerin, Isopropyl Palmitate, Polyglyceryl-4 Diisostearate/ Polyhydroxystearate/Sebacate, Isopropyl Myristate, Magnesium Sulfate, Tocopherol, Polyglyceryl-3 Polyricinoleate, Decylene Glycol, Camellia Sinensis Leaf Extract, Lecithin, Aloe Barbadensis Leaf Juice, Helianthus Annuus (Sunfl ower) Seed Oil, 1,2-Hexanediol, Xanthan Gum, Hydrogenated Castor Oil, Euphorbia Cerifera (Candelilla) Wax/Euphorbia Cerifera Cera/Cire de candelilla, Sodium Chloride, Isostearic Acid, Silica, Polyhydroxystearic Acid, Sodium Benzoate, Potassium Sorbate, Phenoxyethanol, Citric Acid.
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INGREDIENTS AND APPEARANCE
SOLAIRE PEAU PARFAITE MINERAL SCREEN SPF 30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63505-771 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 190 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCO-CAPRYLATE (UNII: 4828G836N6) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETEARYL ISONONANOATE (UNII: P5O01U99NI) ETHYLHEXYL PALMITATE (UNII: 2865993309) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) TOCOPHEROL (UNII: R0ZB2556P8) DECYLENE GLYCOL (UNII: S57M60MI88) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ALOE VERA LEAF (UNII: ZY81Z83H0X) SUNFLOWER OIL (UNII: 3W1JG795YI) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) XANTHAN GUM (UNII: TTV12P4NEE) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) CANDELILLA WAX (UNII: WL0328HX19) SODIUM CHLORIDE (UNII: 451W47IQ8X) ISOSTEARIC ACID (UNII: X33R8U0062) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63505-771-00 1 in 1 CARTON 09/01/2022 02/28/2026 1 148 mL in 1 TUBE; 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 09/01/2022 02/28/2026 Labeler - Yves Rocher North America Inc. (201826448)
