Label: LOREAL PARIS TRUE MATCH NATURALE GENTLE MINERAL MAKEUP BROAD SPECTRUM SPF 19- titanium dioxide powder
- NDC Code(s): 49967-425-01
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 2, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For sunscreen use:
● apply liberally 15 minutes before sun exposure
● reapply at least every 2 hours
● use a water resistant sunscreen if swimming or sweating
● 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
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LOREAL PARIS TRUE MATCH NATURALE GENTLE MINERAL MAKEUP BROAD SPECTRUM SPF 19
titanium dioxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-425 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 100 mg in 1 g Inactive Ingredients Ingredient Name Strength BORON NITRIDE (UNII: 2U4T60A6YD) KAOLIN (UNII: 24H4NWX5CO) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) CARNAUBA WAX (UNII: R12CBM0EIZ) CALCIUM GLUCONATE (UNII: SQE6VB453K) MANGANESE GLUCONATE (UNII: 9YY2F980SV) MAGNESIUM GLUCONATE (UNII: T42NAD2KHC) COPPER PIDOLATE (UNII: 497G7G1SL1) ALOE VERA LEAF (UNII: ZY81Z83H0X) TOCOPHEROL (UNII: R0ZB2556P8) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) MICA (UNII: V8A1AW0880) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-425-01 10 g in 1 JAR; Type 0: Not a Combination Product 07/01/2006 04/30/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/01/2006 04/30/2026 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 062801407 manufacture(49967-425) , pack(49967-425)
