Vertra Mineral Sunscreen Lotion Broad Spectrum SPF 50

Manufacturer
Eai-jr 286, Inc
Effective date
2025-03-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:57:46

Label at a glance#

ProductVertra Mineral Sunscreen Broad Spectrum SPF 50
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Zinc Oxide 23%.....Sunscreen

OTC - PURPOSE SECTION

Uses

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If product is swallowed, get medical help or contact a Poison Control Center Right away.

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if

  • rash occurs

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

DOSAGE & ADMINISTRATION SECTION

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
  • 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: Ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Caprylyl Caprylate/Caprate, Capric/ Caprylic Triglyceride, Coco-Caprylate, Polyglyceryl-2 Oleate, Polyhydroxystearic Oleate, Polyhydroxystearic Acid, Hydrogenated Methyl Abietate, Glycerin, Magnesium Sulfate, Glyceryl Caprylate, Laminaria Digitata (Sea Kelp) Extract, Cucumis Sativus (Cucumber) Fruit Extract, Undaria Pinnatifida (Wakame) Cell Culture Extract, Polyglyceryl-2 Stearate, Galactoarabinan, Triethoxycaprylylsilane, Ethylhexyl Palmitate, Aloe Barbadensis Innter Leaf Extract, Diheptyl Succinate, Capryloyl Glycerin/Sebacic Acid Copolymer, Oryza Sativa (Rice) Bran Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Helianthus Annuus (Sunflower) Extract, Tocopherol, Caprylhydroxamic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mineral Body Lotion SPF 50Mineral Body Lotion SPF 50

vertra

50

Mineral

Sunscreen Lotion

Broad Spectrum SPF 50

Water Resistant (80 Minutes)

Suitable for Face & Body

3 FL OZ / 89 mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71014-042-01Vertra Mineral Sunscreen Broad Spectrum SPF 5089 mL in 1 BOTTLELOTION891

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71014-042VERTRA MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 (ZINC OXIDE) LOTION [EAI-JR 286, INC]1Current NDC, 1 package rows20250327_30caf1dd-142d-85d3-e063-6394a90a0c88.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71014-04271014-042-01

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
Vertra Mineral Sunscreen Broad Spectrum SPF 50ZINC OXIDEEai-jr 286, Inc30caf1dd-142d-85d3-e063-6394a90a0c882025-03-20WarningsExact identifier
ndc (package): 71014-042-01
ndc (product): 71014-042
ndc11 (package): 71014004201
spl id: 30caf1dd-142e-85d3-e063-6394a90a0c88
spl set id: 30caf1dd-142d-85d3-e063-6394a90a0c88

Reported adverse events (FAERS/openFDA)#

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