Label: MAYBELLINE NEW YORK MASTER PRIME BY FACE STUDIO PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN- octinoxate lotion
- NDC Code(s): 49967-196-01
- Packager: L’Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 28, 2023
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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:
● shake well● 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
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Inactive ingredients
water, cyclohexasiloxane, propylene glycol, glycerin, octyldodecanol, stearic acid, potassium cetyl phosphate, palmitic acid, PEG-100 stearate, glyceryl stearate, triethanolamine, phenoxyethanol, cetyl alcohol, talc, dimethicone, silica, methylparaben, caprylyl glycol, carbomer, fragrance, ethylparaben, capryloyl salicylic acid, xanthan gum, disodium EDTA, butylphenyl methylpropional, hexyl cinnamal, linalool, sodium palmitoyl proline, limonene, benzyl salicylate, benzyl alcohol, citronellol, hydroxycitronellal, prunus cerasus (bitter cherry) extract, rosa centifolia flower extract, nymphaea alba flower extract; may contain: mica, titanium dioxide, bismuth oxychloride, iron oxides, red 4, yellow 5
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- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MAYBELLINE NEW YORK MASTER PRIME BY FACE STUDIO PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN
octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-196 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) OCTYLDODECANOL (UNII: 461N1O614Y) STEARIC ACID (UNII: 4ELV7Z65AP) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) PALMITIC ACID (UNII: 2V16EO95H1) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) TROLAMINE (UNII: 9O3K93S3TK) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETYL ALCOHOL (UNII: 936JST6JCN) TALC (UNII: 7SEV7J4R1U) DIMETHICONE (UNII: 92RU3N3Y1O) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) METHYLPARABEN (UNII: A2I8C7HI9T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) ETHYLPARABEN (UNII: 14255EXE39) CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LINALOOL, (+/-)- (UNII: D81QY6I88E) SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO) LIMONENE, (+/-)- (UNII: 9MC3I34447) BENZYL SALICYLATE (UNII: WAO5MNK9TU) BENZYL ALCOHOL (UNII: LKG8494WBH) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) PRUNUS CERASUS FLOWER BUD (UNII: 1MG3D59XD7) ROSA CENTIFOLIA FLOWER (UNII: CS4TE8FF7O) NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) FERRIC OXIDE RED (UNII: 1K09F3G675) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-196-01 30 mL in 1 TUBE; Type 0: Not a Combination Product 07/31/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/31/2014 Labeler - L’Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L’Oreal USA, Inc. 624244349 manufacture(49967-196)
