FACE VALUES WET N DRY WET SKIN SUNSCREEN SPF 50- avobenzone, homosalate, octisalate, octocrylene spray 
HARMON STORES, 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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FACE VALUES WET N' DRY WET SKIN SUNSCREEN SPRAY SPF 50

Active ingredients

Avobenzone 3.0%, Homosalate, 8.0%, Octisalate 4.0%, Octocrylene 8.0%

Purpose

Sunscreen

Uses

Warnings

For external use only

FLAMMABLE:

Do not use

• on damaged or broken skin.

When using this product

• keep out of eyes. Rinse with water to remove. • do not puncture or incinerate. Contents under pressure. • do not store at temperatures above 120°F.

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

   • after 80 minutes of swimming or sweating

   • immediately after towel drying

   • at least every 2 hours

   • limit time in the sun, especially from 10 a.m. - 2 p.m.

   • wear long-sleeved shirts, pants, hats, and sunglasses

Other information

Inactive ingredients

alcohol denat., cyclopentasiloxane, tridecyl salicylate, octyldodecyl citrate crosspolymer, trimethylpentanediol/adipic acid/glycerin crosspolymer, ethyl methicone, bis-hydroxyethoxypropyl dimethicone, acrylates/dimethicone copolymer, fragrance, tocopheryl acetate, nelumbo nucifera flower extract, ascorbyl palmitate, propylene glcol

Label

42136D3

FACE VALUES WET N DRY WET SKIN SUNSCREEN SPF 50 
avobenzone, homosalate, octisalate, octocrylene spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-085
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M)  
ALCOHOL (UNII: 3K9958V90M)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M)  
TRIMETHYLPENTANEDIOL/ADIPIC ACID/GLYCERIN CROSSPOLYMER (25000 MPA.S) (UNII: 587WKM3S9Q)  
ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H)  
BIS-HYDROXYETHOXYPROPYL DIMETHICONE (50 CST) (UNII: YP714N2H05)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63940-085-10283 g in 1 CAN; Type 0: Not a Combination Product07/02/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35207/02/2021
Labeler - HARMON STORES, INC. (804085293)

Revised: 12/2022
Document Id: f071a44f-c122-3afc-e053-2995a90adf5b
Set id: f071a899-83f5-3323-e053-2a95a90af46e
Version: 1
Effective Time: 20221222
 
HARMON STORES, INC.