FDA.reportPublic FDA data

Badger SPF 34 Anti-Bug Sunscreen

Manufacturer
Norwood Packaging Ltd.
Effective date
2014-01-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:38:10

Label at a glance#

ProductBadger SPF 34 Anti-Bug Sunscreen
Active ingredientZINC OXIDE
Label structure8 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. After 40 minutes of swimming or sweating Immediately after towel drying At least every 2 hours Spending time in the sun increases your risk of skin cancer and early skin aging To decrease this risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or highe...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Sunscreen Ingredient

OTC - ACTIVE INGREDIENT SECTION

Non-Nano Uncoated Zinc Oxide 20%

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.

Caution

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin. Prolonged or frequently repeated skin contact may cause allergic reactions in some individuals. 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 swallowed, get medical help or contact a poison control center right away.

  • Adult supervision required.
  • Do not apply to children's hands.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For full protection, apply liberally (2mg/cm2 of skin) to all exposed skin 15 minutes before sun exposure, then rub in to reduce whitening effect.

Reapply

SPL UNCLASSIFIED SECTION

  • After 40 minutes of swimming or sweating
  • Immediately after towel drying
  • At least every 2 hours

Sun Protection Measures

SPL UNCLASSIFIED SECTION

  • Spending time in the sun increases your risk of skin cancer and early skin aging
  • To decrease this risk, regularly use a sunscreen with 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

1Olea Europaea (Extra Virgin Olive) Oil, 1Cera Alba (Beeswax), 1Ricinus Communis (Castor) Oil, 1Cymbopogon Nardus (Citronella) Oil, 1Cymbopogon Schoenanthus (Lemongrass) Oil, 1Cedrus Deodara (Cedar) Oil,1Rosmarinus Officinalis (Rosemary) Oil, and 1Pelargonium Graveolens (Geranium) Oil.

1 =Certified Organic

PRINCIPAL DISPLAY PANEL - 87 ml Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Active

BADGER®

DEET
FREE

Citronella & Cedar

Broad Spectrum
SPF 34

ANTI-BUG
SUNSCREEN

Tested to Repel Mosquitoes
Certified Natural • Contains 98% Organic Ingredients

WATER
RESISTANT
40 min

UVA
UVB

NON
NANO

BIO
DEGRADABLE

ACTIVE ANTI-BUG INGREDIENTS (15.5%): 10% *Castor Oil,
& Essential Oils of 2.5% *Citronella, 1.25% *Lemongrass,
1% *Cedar, 0.5% *Rosemary, & 0.25% *Geranium.

OTHER INGREDIENTS (84.5%): *Extra Virgin Olive Oil,
Zinc Oxide, *Beeswax. *= Certified Organic

87ml/2.9 fl.oz

PRINCIPAL DISPLAY PANEL - 87 ml Tube Label
PRINCIPAL DISPLAY PANEL - 87 ml Tube Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55143-103-012019-11-27C16284748780-19855e2a2-4cd7-60a7-e053-dbdaa90a05bdBadger ® SPF 34 Anti-Bug Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55143-103-01Badger SPF 34 Anti-Bug Sunscreen87 mL in 1 TUBECREAM871

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55143-103BADGER SPF 34 ANTI-BUG SUNSCREEN (ZINC OXIDE) CREAM [NORWOOD PACKAGING LTD.]1Legacy NDC, 1 package rows20140117_d9aa07df-c4df-412c-a7f9-321b6f58c0a1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1
CASTOR OILINACTIVE INGREDIENTD5340Y2I9G1
CEDRUS DEODARA WOODINACTIVE INGREDIENT1GO876QOY21
CITRONELLA OILINACTIVE INGREDIENTQYO8Q067D01
GERANIUM OIL, ALGERIAN TYPEINACTIVE INGREDIENT5Q1I94P4WG1
OLIVE OILINACTIVE INGREDIENT6UYK2W1W1E1
ROSEMARY OILINACTIVE INGREDIENT8LGU7VM3931
WEST INDIAN LEMONGRASS OILINACTIVE INGREDIENT5BIA40E9ED1
YELLOW WAXINACTIVE INGREDIENT2ZA36H0S2V1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55143-10355143-103-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
OLIVE OIL6UYK2W1W1EIACT
YELLOW WAX2ZA36H0S2VIACT
CASTOR OILD5340Y2I9GIACT
CITRONELLA OILQYO8Q067D0IACT
CEDRUS DEODARA WOOD1GO876QOY2IACT
ROSEMARY OIL8LGU7VM393IACT
WEST INDIAN LEMONGRASS OIL5BIA40E9EDIACT
GERANIUM OIL, ALGERIAN TYPE5Q1I94P4WGIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 30 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, COATED / ORAL213.7 mgExact identifier — unii candidate
9 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, FILM COATED / ORAL15.29 mgExact identifier — unii candidate
16 equally ranked IID candidates
OLIVE OILOLIVE OIL6UYK2W1W1ECAPSULE / ORALNAExact identifier — unii candidate
5 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GINJECTION / INTRAMUSCULAR885 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, DELAYED RELEASE / ORAL0.01 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GINJECTION, SOLUTION / INTRAMUSCULAR525 mgExact identifier — unii candidate
16 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, DELAYED RELEASE / ORAL0.1 mgExact identifier — unii candidate
9 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET / ORAL17 mgExact identifier — unii candidate
16 equally ranked IID candidates
OLIVE OILOLIVE OIL6UYK2W1W1ELOTION / TOPICAL32468 mgExact identifier — unii candidate
5 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VCAPSULE / ORAL44 mgExact identifier — unii candidate
9 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GCAPSULE / ORAL1.04 mgExact identifier — unii candidate
16 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, EXTENDED RELEASE / ORAL0.01 mgExact identifier — unii candidate
9 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GEMULSION / OPHTHALMIC32 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GGEL / NASAL429 mgExact identifier — unii candidate
16 equally ranked IID candidates
OLIVE OILOLIVE OIL6UYK2W1W1ESOLUTION / TOPICAL0.6 %w/wExact identifier — unii candidate
5 equally ranked IID candidates
OLIVE OILOLIVE OIL6UYK2W1W1ESOAP / TOPICALNAExact identifier — unii candidate
5 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GSPRAY / NASALNAExact identifier — unii candidate
16 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VCAPSULE, EXTENDED RELEASE / ORAL80.67 mgExact identifier — unii candidate
9 equally ranked IID candidates
OLIVE OILOLIVE OIL6UYK2W1W1ESOLUTION / ORAL425 mg/1mlExact identifier — unii candidate
5 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VCREAM / TOPICAL5 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, EXTENDED RELEASE / ORAL23.27 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET / SUBLINGUAL1.6 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, COATED / ORAL0.9 mgExact identifier — unii candidate
16 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VOINTMENT / TOPICAL20 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET / ORAL3.22 mgExact identifier — unii candidate
9 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GCAPSULE, EXTENDED RELEASE / ORAL47 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GGRANULE, FOR SUSPENSION / ORAL128 mgExact identifier — unii candidate
16 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, SUGAR COATED / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates

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
40043922-9aaf-4aac-983a-a20224ab6da3d9aa07df-c4df-412c-a7f9-321b6f58c0a12014-01-13WarningsExact identifier
spl id: 40043922-9aaf-4aac-983a-a20224ab6da3
spl set id: d9aa07df-c4df-412c-a7f9-321b6f58c0a1

Reported adverse events (FAERS/openFDA)#

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