ETERNAL SPIRIT BEAUTY SPF 50SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone spray 
Prime Enterprises 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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Eternal beauty Sunscreen Spray SPF 50 Broad Spectrum

Active ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 2.75%

Oxybenzone 4%

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. Keep away from face to avoid breathing it.

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.

Flammable: Do not use near heat, flame or while smoking.

Directions:

Inactive ingredients:

SD Alcohol 40-B, Cyclopentasiloxane, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Water, Silica Silylate, Rosa Damascena Flower Water, Mentha Viridis (Spearmint) Leaf Oil, Bisabolol, Polyester-8, Tocopheryl Acetate, Ascorbyl Palmitate, Glycerin, Camellia Oleifera (Green Tea) Leaf Extract, Benzyl Alcohol, Aloe Barbadensis Leaf Juice Powder, Dehydroacetic Acid, Sodium Hyaluronate.

Other Information:

Question or comments?

Call 1-866-983-8582

Eteral Spirit Beauty Sunscreen Spray SPF 50

Principal Display Label

ETERNAL SPIRIT BEAUTY  SPF 50SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58443-0339
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE26.4 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE88 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE44 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE24.2 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE35.2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
SPEARMINT OIL (UNII: C3M81465G5)  
ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)  
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
WATER (UNII: 059QF0KO0R)  
ISOBORNYL ACRYLATE (UNII: IX0PRH184P)  
ALCOHOL (UNII: 3K9958V90M)  
LEVOMENOL (UNII: 24WE03BX2T)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Product Characteristics
Coloryellow (Very light yellow) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58443-0339-3118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/11/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35201/11/2018
Labeler - Prime Enterprises Inc. (101946028)
Registrant - Prime Enterprises Inc. (101946028)
Establishment
NameAddressID/FEIBusiness Operations
Prime Enterprises Inc101946028manufacture(58443-0339) , analysis(58443-0339) , pack(58443-0339) , label(58443-0339)

Revised: 6/2020
Document Id: a8739ddd-c228-44e0-e053-2a95a90a9dca
Set id: a873a5ff-910a-f0e5-e053-2995a90a88c3
Version: 1
Effective Time: 20200619
 
Prime Enterprises Inc.