CVS HEALTH SPF 30 ULTRA SHEER- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion 
CVS PHARMACY

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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CVS Health SPF 30 Ultra Sheer Lotion

Active ingredients

Avobenzone 3.0%, Homosalate 8.0%, Octisalate 5.0%, Octocrylene 4.0%, Oxybenzone 4.0%

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

Other information

Inactive ingredients

water, silica, dimethicone, potassium cetyl phosphate, beeswax, benzyl alcohol, glyceryl stearate, PEG-100 stearate, cetyl dimethicone, caprylyl methicone, caprylyl glycol, ethyhexylglycerin, dimethicone/PEG-10/15 crosspolymer, sodium polyacrylate, behenyl alcohol, xanthan gum, ethylhexyl stearate, acrylates/C12-22 alkyl methacrylate copolymer, disodium EDTA, chlorphenesin, fragrance, BHT, trideceth-6, propylene glycol

Label

CVS59034A

CVS57369A

CVS HEALTH SPF 30 ULTRA SHEER 
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-028
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE80 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE40 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE40 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DOCOSANOL (UNII: 9G1OE216XY)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PEG-100 STEARATE (UNII: YD01N1999R)  
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CETYL DIMETHICONE 45 (UNII: IK315POC44)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
WATER (UNII: 059QF0KO0R)  
WHITE WAX (UNII: 7G1J5DA97F)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51316-028-0989 mL in 1 TUBE; Type 0: Not a Combination Product02/07/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35202/07/2017
Labeler - CVS PHARMACY (062312574)

Revised: 1/2023
Document Id: f32dc488-6686-5a77-e053-2995a90a544b
Set id: f32d551a-c7b2-6492-e053-2995a90a4322
Version: 1
Effective Time: 20230126
 
CVS PHARMACY