NOEVIR RAYSELA UV SHIELD PRIMER- zinc oxide, octinoxate cream 
Nippon Shikizai, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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NOEVIR RAYSELA
UV SHIELD PRIMER
RAYSELA Base Protection UV
BROAD SPECTRUM
SPF50+

Protects skins from the sun's harmful rays (UV-A, UV-B) to prevent sunburn, spots and premature signs of aging while keeping your skin hydrated.

Drug Facts

Active Ingredients

OCTINOXATE 6.99%

ZINC OXIDE 17.67%

Purpose

Sunscreen

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

Directions

For sunscreen use:

Other Information

Inactive ingredients

WATER, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, DIPHENYLSILOXY PHENYL TRIMETHICONE, PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, POLYMETHYLSILSESQUIOXANE, DISTEARDIMONIUM HECTORITE, HYDROGEN DIMETHICONE, PENTYLENE GLYCOL, GLYCERIN, MAGNESIUM SULFATE, POLYHYDROXYSTEARIC ACID, SORBITAN SESQUIISOSTEARATE, TRIMETHYLSILOXYSILICATE, SILICA DIMETHYL SILYLATE, SODIUM CITRATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, TOCOPHEROL, SQUALANE, ALCOHOL, CELLULOSE ACETATE, ASCOPHYLLUM NODOSUM EXTRACT, SORBITOL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, PHELLODENDRON AMURENSE BARK EXRACT, BELAMCANDA CHINENSIS ROOT EXTRACT, VITIS VINIFERA (GRAPE) LEAF EXTRACT, CITRUS GRANDIS (GRAPEFRUIT) FRUIT EXTRACT, SPIRAEA ULMARIA FLOWER EXTRACT, PHENOXYETHANOL, FRAGRANCE

Principal Display Panel - Raysela UV Shield Primer Label

RAYSELA

UV Shield Primer

Base Protection UV

BROAD
SPECTRUM

SPF
50+

NOEVIR

NET WT. 1.7 OZ. - 50g

Principal Display Panel - Raysela UV Shield Primer Label
NOEVIR RAYSELA UV SHIELD PRIMER 
zinc oxide, octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24509-0001
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE176.7 mg  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE69.9 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)  
PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)  
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)  
GLYCERIN (UNII: PDC6A3C0OX)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
SORBITAN SESQUIISOSTEARATE (UNII: VU97D01BF9)  
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)  
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SQUALANE (UNII: GW89575KF9)  
TOCOPHEROL (UNII: R0ZB2556P8)  
CELLULOSE ACETATE (UNII: 3J2P07GVB6)  
ROSEMARY (UNII: IJ67X351P9)  
ALCOHOL (UNII: 3K9958V90M)  
PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)  
PUMMELO (UNII: ET1TN5W71X)  
FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)  
IRIS DOMESTICA ROOT (UNII: T2MU9QFA87)  
VITIS VINIFERA LEAF (UNII: R1H893D80E)  
ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)  
SORBITOL (UNII: 506T60A25R)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24509-0001-11 in 1 BOX04/10/2018
150 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35204/10/2018
Labeler - Nippon Shikizai, Inc. (692572936)
Establishment
NameAddressID/FEIBusiness Operations
Nippon Shikizai, Inc.692076308MANUFACTURE(24509-0001) , ANALYSIS(24509-0001) , PACK(24509-0001) , LABEL(24509-0001)

Revised: 1/2021
Document Id: 71425e13-a20e-4ddc-b61b-5436a5ab017e
Set id: 45030b2f-21cf-4285-af12-87ea8f0b8df7
Version: 7
Effective Time: 20210107
 
Nippon Shikizai, Inc.