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

CVS Health 50 Hydrating Mineral Sunscreen by

Drug Labeling and Warnings

CVS Health 50 Hydrating Mineral Sunscreen by is a Otc medication manufactured, distributed, or labeled by CVS PHARMACY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Titanium Dioxide 9.0%, Zinc Oxide 7.0%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see  Directions), decreases the risk of skin cancer and early skin aging caused by the sun

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

• apply liberally 15 minutes before sun exposure
• use a water resistant sunscreen if swimming or sweating
• reapply at least every 2 hours
• children under 6 months of age: Ask a doctor
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

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

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

Other information

• protect the product in this container from excessive heat and direct sun
• may stain or damage some fabrics, materials or surfaces

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

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-046
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	90 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	70 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-046-15	150 mL in 1 TUBE; Type 0: Not a Combination Product	12/09/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/09/2019	07/28/2025

Labeler - CVS PHARMACY (062312574)