Meijer SPF 50 Sunscreen

Manufacturer
Meijer | Derma Care Research Labs, LLC
Effective date
2024-02-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:12:45

Label at a glance#

ProductMeijer SPF 50 Sunscreen
Active ingredientHOMOSALATE, AVOBENZONE, OCTOCRYLENE, OCTISALATE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 15%, Ocitsalate 5%, Octocrylene 10%

OTC - PURPOSE SECTION

Sunscreen

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 SECTION

For external use only.

Do not use on damaged or broken skin.

When using this product avoid contact with eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure and as needed. Reapply: after 80 minutes of swimming or sweating, immediately after towel drying, at least every 2 hours.

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, children under 6 months of age: ask a doctor.

INACTIVE INGREDIENT SECTION

Water, sorbitol, aluminum starch octenylsuccinate, VP/Eicosense copolymer, stearic acid, dimethicone, tocopherol, ethylhexylglycerin, phenoxyethanol, polyglyeryl-3 distearate, sorbitan isostearate, carbomer, disodium EDTA, triethanolamine, benzyl alcohol, fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-1830-8Meijer SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2272
79481-1830-9Meijer SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2272

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-1830MEIJER SPF 50 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 10%) LOTION [MEIJER]2Current NDC, 2 package rows20240522_075dddd5-46ea-282a-e063-6294a90a28fd.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-183079481-1830-8, 79481-1830-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
Meijer SPF 50 SunscreenAVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 10%Meijer075dddd5-46ea-282a-e063-6294a90a28fd2024-02-15WarningsExact identifier
ndc (package): 79481-1830-8
ndc (package): 79481-1830-9
ndc (product): 79481-1830
ndc11 (package): 79481183009
ndc11 (package): 79481183008
spl id: 117293c0-9d8d-5856-e063-6394a90a42fe
spl set id: 075dddd5-46ea-282a-e063-6294a90a28fd

Reported adverse events (FAERS/openFDA)#

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