CVS HEALTH 50 HYDRATING MINERAL SUNSCREEN- titanium dioxide, zinc oxide lotion 
CVS PHARMACY

----------

CVS Health 50 Hydrating Mineral Sunscreen

Active ingredients

Titanium Dioxide 9.0%, Zinc Oxide 7.0%

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

• 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

WATER, ISOHEXADECANE, BUTYLOCTYL SALICYLATE, CETYL DIMETHICONE, STYRENE/ACRYLATES COPOLYMER, OLIVE OIL POLYGLYCERYL-6 ESTERS, SORBITAN OLIVATE, SODIUM STEAROYL LACTYLATE, VP/EICOSENE COPOLYMER, CETEARYL ALCOHOL, CETEARYL OLIVATE, CETYL PALMITATE, SORBITAN PALMITATE, DIMETHICONE PEG-8 LAURATE, CERAMIDE NP, CERAMIDE AP, CERAMIDE EOP, CHOLESTEROL, PHYTOSPHINGOSINE, HYDROLYZED HYALURONIC ACID, BENZYL ALCOHOL, BISABOLOL, DIPOTASSIUM GLYCYRRHIZATE, PROPANEDIOL, XANTHAN GUM, ALUMINUM HYDROXIDE, SODIUM LAUROYL LACTYLATE, CARBOMER, TOCOPHERYL ACETATE, DISODIUM EDTA, STEARIC ACID, TRIETHOXYCAPRYLYLSILANE, CITRIC ACID, PHENOXYETHANOL, CAPRYLOYL GLYCINE, UNDECYLENOYL GLYCINE.

Label

CVS62392A

CVS HEALTH 50 HYDRATING MINERAL SUNSCREEN 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-046
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE90 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE70 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
LEVOMENOL (UNII: 24WE03BX2T)  
CETYL DIMETHICONE 45 (UNII: IK315POC44)  
DIMETHICONE PEG-8 LAURATE (UNII: 72MF9C2A18)  
FARNESOL (UNII: EB41QIU6JL)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CERAMIDE NP (UNII: 4370DF050B)  
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
CERAMIDE AP (UNII: F1X8L2B00J)  
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
UNDECYLENOYL GLYCINE (UNII: 4D20464K2J)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
XANTHAN GUM (UNII: TTV12P4NEE)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
WATER (UNII: 059QF0KO0R)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
OLIVE OIL POLYGLYCERYL-6 ESTERS (UNII: 4KDO9AFM9I)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)  
PROPANEDIOL (UNII: 5965N8W85T)  
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51316-046-15150 mL in 1 TUBE; Type 0: Not a Combination Product12/09/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02012/09/201907/28/2025
Labeler - CVS PHARMACY (062312574)

Revised: 10/2024
Document Id: 24af4395-249b-3a0a-e063-6394a90af0d5
Set id: fa2c8dc3-f6df-3122-e053-6394a90a95fa
Version: 2
Effective Time: 20241017
 
CVS PHARMACY