MAYBELLINE NEW YORK MASTER PRIME BY FACE STUDIO PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN- octinoxate lotion 
L’Oreal USA Products Inc

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Drug Facts

Active ingredient

Octinoxate 7.5%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

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

protect the product in this container from excessive heat and direct sun

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

Questions or comments?

1-800-944-0730

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MAYBELLINE NEW YORK MASTER PRIME BY FACE STUDIO PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN 
octinoxate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-196
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-196-0130 mL in 1 TUBE; Type 0: Not a Combination Product07/31/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02007/31/2014
Labeler - L’Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L’Oreal USA, Inc.624244349manufacture(49967-196)

Revised: 12/2023
Document Id: cc4d39ba-60d8-4a85-96f7-faadfc3b1ab3
Set id: feabb713-4ef1-45b3-b34f-562e37b314d5
Version: 4
Effective Time: 20231228
 
L’Oreal USA Products Inc