FDA.reportPublic FDA data

Equate beauty ultra light Suncreen SPF 55

Manufacturer
Walmart Stores iNC. | Fruit of the Earth Inc.
Effective date
2019-02-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:31:09

Label at a glance#

ProductEquate beauty ultra light Suncreen SPF 55
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure9 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 skin 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 of 15 or higher and othe...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Homosalate 10.0%

Octisalate 3.0%

Octocrylene 7.0%

Oxybenzone 6.0%

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 skin aging caused by the sun

Warnings

WARNINGS SECTION

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

OTC - ASK DOCTOR 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 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

SPL UNCLASSIFIED SECTION

• protect this product from excessive heat and direct sun

• may stain or damage some fabrics, materials or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, butyloctyl salicylate, styrene/acrylates copolymer, silica, VP/hexadecene copolymer, caprylyl dimethicone, polysilicone 15, behenyl alcohol,

glyceryl stearate, ethylhexylglycerin, propylene glycol, canola oil, PEG-100 stearate, dimethicone, sodium polyacrylate, rosmarinus officinalis (rosemary) leaf extract, ethylhexyl stearate, trimethylsiloxysilicate, trideceth-6, xanthan gum, iodopropynyl butylcarbamate, phenoxyethanol, disodium EDTA, fragrance

Prinicipal Dispaly panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionEquate beauty

Compare to NEUTROGENA ULTRA SHEER ® DRY-TOUCH*

Ultra Light Sunscreen  LOTION

SPF 55

Broad Spectrum SPF 55 Light, clean & oil-free Water resistant (80 minutes) Dermatologist tested

PARABEN FREE *

3 FL OZ (89 mL)

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
49035-63949035-639-09

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OXYBENZONE95OOS7VE0YACTIB
WATER059QF0KO0RIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW)5Z4DPO246AIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
VINYLPYRROLIDONE/HEXADECENE COPOLYMERKFR5QEN0N9IACT
DIMETHICONE92RU3N3Y1OIACT
POLYSILICONE-15F8DRP5BB29IACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CANOLA OIL331KBJ17RKIACT
PEG-100 STEARATEYD01N1999RIACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
ROSEMARYIJ67X351P9IACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
TRIMETHYLSILOXYSILICATE (M/Q 0.66)5041RX63GNIACT
TRIDECETH-63T5PCR2H0CIACT
XANTHAN GUMTTV12P4NEEIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DISODIUM EDTA-COPPER6V475AX06UIACT

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
6629a791-f0d2-4f0e-b7d8-b937aef7f087bbef11ff-85b4-45ce-85a3-4be489a763882019-02-12WarningsExact identifier
spl id: 6629a791-f0d2-4f0e-b7d8-b937aef7f087
spl set id: bbef11ff-85b4-45ce-85a3-4be489a76388

Reported adverse events (FAERS/openFDA)#

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