EQUATE ZIINC SUNSCREEN ULTRA BROAD SPECTRUM- octinoxate, titanium dioxide, zinc oxide cream 
Walmart 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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Equate Zinc Sunscreen ULTRA Broad Spectrum

Active ingredients

Octinoxate 4.0%

Titanium Dioxide 5.0%

Zinc Oxide 9.1%

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

• reapply:

   • after 80 minutes of swimming or sweating

   • immediately after towel drying

   • 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 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-sleeve shirts, pants, hats, and sunglasses

Other information

• protect this product from excessive heat and direct sun

• may stain or damage some fabrics/materials or surfaces

Inactiveingredients

water, C12-15 alkyl benzoate, cetyl dimethicone, cetyl PEG/PPG-10/1 dimethicone, caprylic/capric triglyceride, ethylhexyl palmitate, tridecyl salicylate, polyethylene, tetradecane, hydrogenated castor oil, hydrogenated polydecene, aloe barbadensis leaf juice, butylene glycol, ethylhexyl stearate, cyclopentasiloxane, cyclohexsiloxane, caprylyl glycol, phenoxyethanol, hydroxyethylcellulose, tetrahexyldecyl ascorbate, triethoxycaprylylsilane, hexylene glycol, dimethicone, tocopheryl acetate, camellia sinensis (green tea) leaf extract, sodium chloride

49035-564-42

EQUATE ZIINC SUNSCREEN ULTRA BROAD SPECTRUM 
octinoxate, titanium dioxide, zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-564
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE40 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE50 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION91 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
TETRADECANE (UNII: 03LY784Y58)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-564-431 in 1 PACKAGE02/20/2019
1NDC:49035-564-4229.6 mL in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35202/20/2019
Labeler - Walmart Stores Inc. (051957769)

Revised: 10/2021
Document Id: cebc37a2-360a-e68d-e053-2a95a90a2ab8
Set id: 7123a744-1715-49ab-8d6d-4baeabe61cb5
Version: 9
Effective Time: 20211019
 
Walmart Stores Inc.