Equate

Manufacturer
Wal-Mart Stores, Inc.
Effective date
2021-11-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:29:25

Label at a glance#

ProductEquate
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure9 sections

Storage and handling

Other information   •protect the product in this container from excessive heat and direct sun.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Avobenzone, 2.0%

Homosalate, 7.0%

Octisalate, 4.0%

Octocrylene, 1.5%

Oxybenzone, 2.0%

OTC - PURPOSE SECTION

Purpose

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Sunscreen

INDICATIONS & USAGE SECTION

Uses   •helps prevent sunburn

•if used as directed with other sun protection measres

(see Directions), decreases the risk of skin cancer and

early skin aging caused by the sun.

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical

help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions •apply liberally 15 minutes before sun

exposure  •reapply at least every 2 hours  •use water

resistant sunscrenn if swimming or sweating  •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 SpectrumSPF

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.

STORAGE AND HANDLING SECTION

Other information  •protect the product in this

container from excessive heat and direct sun.

INACTIVE INGREDIENT SECTION

Inactive ingredients  Water, Glycerin, C12-15 Alkyl Benzoate, Cetearyl Alcohol,

Silica, Arachidyl Alcohol, Behenyl Alcohol, Arachidyl Glucoside, Glyceryl Stearate,

PEG-100 Stearate, Diethylhexyl 2,6-Naphthalate, Cetearyl Glucoside,

Phenoxyethanol, Ethylhexylglycerin, Dimethicone, Polysorbate 20,

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine,

Retinyl Palmitate, Dipotassium Glycyrrhizate, Hyaluronic Acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-81649035-816-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

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
fe6a2a71-4dbc-ce7f-e053-6394a90a94d0daca3878-e854-47dc-8632-12563bf4bce62023-06-18WarningsExact identifier
spl set id: daca3878-e854-47dc-8632-12563bf4bce6

Reported adverse events (FAERS/openFDA)#

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