FDA.reportPublic FDA data

Walmart Equate SPF 50 Ultra Sunscreen Lotion

Manufacturer
Wal-Mart Stores Inc
Effective date
2024-10-16
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:26:22

Label at a glance#

ProductEquate SPF 50 Ultra Sunscreen
Active ingredientHOMOSALATE, AVOBENZONE, OCTISALATE, OCTOCRYLENE
Label structure12 sections

Indications and uses

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

Dosage and administration

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 value of 15 or higher and other sun p...

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 7.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

• on damaged or broken skin.

When using this product ​

OTC - WHEN USING SECTION

• keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

• rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, tridecyl salicylate, sorbitol, polyethyloxazoline, stearic acid, triethanolamine, aluminum starch octenylsuccinate, carbomer, polyglyceryl-3 distearate, dimethicone, sorbitan isostearate, fragrance, benzyl alcohol, caprylyl glycol, phenoxyethanol, ethylhexylglycerin, tocopherol (Vitamin E), disodium EDTA.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EQ08159A2EQ08159A2

EQ24772E2EQ24772E2

EQ24772F2EQ24772F2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-759-12EquateSPF 50 Ultra Sunscreen236 mL in 1 TUBELOTION2365
49035-759-14EquateSPF 50 Ultra Sunscreen473 mL in 1 BOTTLE, PLASTICLOTION4735

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-759EQUATE SPF 50 ULTRA SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [WAL-MART STORES INC]5Current NDC, Legacy NDC, 2 package rows20241018_8f02f297-5315-ced4-e053-2a95a90a8c7b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-75949035-759-12, 49035-759-14

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SORBITOL506T60A25RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
STEARIC ACID4ELV7Z65APIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
DIMETHICONE92RU3N3Y1OIACT
BENZYL ALCOHOLLKG8494WBHIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
POLYGLYCERYL-3 DISTEARATEZI1LK470XVIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01IACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
TROLAMINE9O3K93S3TKIACT
EDETATE DISODIUM7FLD91C86KIACT
POLYETHYLOXAZOLINE (500000 MW)S5DPG6K67IIACT
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Equate SPF 50 Ultra SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEWal-Mart Stores Inc8f02f297-5315-ced4-e053-2a95a90a8c7b2024-10-16WarningsExact identifier
ndc (package): 49035-759-14
ndc (package): 49035-759-12
ndc (product): 49035-759
ndc11 (package): 49035075914
ndc11 (package): 49035075912
spl id: 249e9a6e-b52d-0c56-e063-6394a90a6664
spl set id: 8f02f297-5315-ced4-e053-2a95a90a8c7b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.