FDA.reportPublic FDA data

Badger ® Active SPF 30 Clear Zinc Sunscreen Cream

Manufacturer
W.S. Badger Company, Inc.
Effective date
2021-09-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:42:33

Label at a glance#

ProductBadger Active SPF 30 Clear Zinc Sunscreen
Active ingredientZINC OXIDE
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

For full protection, apply liberally (2mg/cm 2 of skin) to all exposed skin 15 minutes before sun exposure, then rub in to reduce whitening effect. 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 bro...

Storage and handling

Store at temperatures below 90°F.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Uncoated Zinc Oxide 18.75%

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 skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin. Stop and ask a doctor if rash occurs.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For full protection, apply liberally (2mg/cm 2 of skin) to all exposed skin 15 minutes before sun exposure, then rub in to reduce whitening effect.

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 10am-2pm
    • Wear long-sleeved shirts, pants, hats, and sunglasses
  • For children under 6 months of age: ask a doctor.

Ingredients

INACTIVE INGREDIENT SECTION

1Helianthus Annuus ( Sunflower) Oil, 1Cera Alba ( Beeswax), Tocopherol ( Sunflower Vitamin E), * Hippophae rhamnoides (Sea Buckthorn) Fruit Extract.

1 = Organic

Other Information

STORAGE AND HANDLING SECTION

Store at temperatures below 90°F.

PRINCIPAL DISPLAY PANEL - 87 ml Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Active

BADGER ®

Unscented

Broad Spectrum
SPF 30

CLEAR ZINC

NATURAL MINERAL
SUNSCREEN CREAM

Non-Whitening

Face & Body

WATER RESISTANT 40min

NON GMO

CLEAR ZINC

REEF FRIENDLY


98% ORGANIC INGREDIENTS

& CLEAR ZINC OXIDE

87ml/2.9 fl.oz

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62206-4710-02025-01-30C16284748780-12cef2736-876d-d83d-e063-dadaa90ab31fBadger ® Active SPF 30 Clear Zinc Sunscreen Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62206-4710-0Badger Active SPF 30 Clear Zinc Sunscreen87 mL in 1 TUBECREAM874

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62206-4710BADGER ACTIVE SPF 30 CLEAR ZINC SUNSCREEN (ZINC OXIDE) CREAM [W.S. BADGER COMPANY, INC.]4Legacy NDC, 1 package rows20211002_64e077ac-2d3b-9abe-e053-2a91aa0a1d7f.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62206-471062206-4710-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUNFLOWER OIL3W1JG795YIIACT
YELLOW WAX2ZA36H0S2VIACT
TOCOPHEROLR0ZB2556P8IACT
ZINC OXIDESOI2LOH54ZACTIB
HIPPOPHAE RHAMNOIDES FRUITAVL0R9111TIACT

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
cd291d22-57ee-387b-e053-2a95a90a308464e077ac-2d3b-9abe-e053-2a91aa0a1d7f2021-09-29WarningsExact identifier
spl id: cd291d22-57ee-387b-e053-2a95a90a3084
spl set id: 64e077ac-2d3b-9abe-e053-2a91aa0a1d7f

Reported adverse events (FAERS/openFDA)#

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