NYX PROFESSIONAL MAKEUP BARE WITH ME DAILY MOISTURIZING PRIMER WITH CANNABIS SATIVA SEED OIL SPF 30- avobenzone, homosalate, octisalate and octocrylene cream 
L'Oreal USA Products Inc

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Drug Facts

Active ingredients

Avobenzone 3%

Homosalate 5%

Octisalate 5%

Octocrylene 7%

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:

●  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, glycerin, silica, dimethicone, PEG-100 stearate, glyceryl stearate, cannabis sativa seed oil, stearic acid, phenoxyethanol, palmitic acid, ammonium polyacryloyldimethyl taurate, steareth-100, phenylethyl resorcinol, caprylyl salicylic acid, caprylyl glycol, xanthan gum, dimethicone/vinyl dimethicone crosspolymer, disodium EDTA, fragrance, sodium hyaluronate, tocopherol, dipropylene glycol, ascorbyl glucoside, myristic acid, sodium palmitoyl proline, sodium hydroxide, centella asiatica extract, butylene glycol, linalool, geraniol, limonene, nymphaea alba flower extract

image of a label
image of a label
NYX PROFESSIONAL MAKEUP BARE WITH ME DAILY MOISTURIZING PRIMER WITH CANNABIS SATIVA SEED OIL SPF 30 
avobenzone, homosalate, octisalate and octocrylene cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-217
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE50 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PEG-100 STEARATE (UNII: YD01N1999R)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PALMITIC ACID (UNII: 2V16EO95H1)  
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: F01RIY4371)  
STEARETH-100 (UNII: 4OH5W9UM87)  
PHENYLETHYL RESORCINOL (UNII: G37UFG162O)  
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
XANTHAN GUM (UNII: TTV12P4NEE)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
TOCOPHEROL (UNII: R0ZB2556P8)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)  
MYRISTIC ACID (UNII: 0I3V7S25AW)  
SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CENTELLA ASIATICA (UNII: 7M867G6T1U)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
LINALOOL, (+)- (UNII: F4VNO44C09)  
GERANIOL (UNII: L837108USY)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-217-011 in 1 CARTON04/01/2020
175 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02004/01/2020
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA Products Inc624244349manufacture(49967-217)

Revised: 1/2024
Document Id: a1aad5e8-75a3-4614-8ee5-36254adf01e3
Set id: 7f960d4c-ad09-4dc8-b272-66e4df26ace8
Version: 5
Effective Time: 20240116
 
L'Oreal USA Products Inc