Zinc Screen Broad Spectrum Sunscreen SPF 40

Manufacturer
Supergoop, LLC
Effective date
2024-12-04
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:40:58

Label at a glance#

ProductZinc Screen Broad Spectrum Sunscreen SPF 40
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Zinc Oxide 13% Sunscreen

OTC - PURPOSE SECTION

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

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 or irritation develops and lasts.

WARNINGS SECTION

Warnings

Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove
For external use only

DOSAGE & ADMINISTRATION SECTION

Directions

Apply generously and evenly 15 minutes before sun exposure
Use a water-resistant sunscreen if swimming or sweating
Reapply 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 your 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

Inactive Ingredients

Water, Tetradecane, Cetearyl Nonanoate, Ethylhexyl Palmitate, Caprylic/Capric Triglyceride, Isopropyl Myristate, Glycerin, Polyglyceryl-3 Diisostearate, Mica, Propanediol, Disteardimonium Hectorite, Gluconolactone, Polyglyceryl-6 Polyricinoleate, Brassica Campestris/Aleurites Fordi Oil Copolymer, Polyhydrostearic Acid, Sodium Chloride, Magnesium Sulfate, Fructose, Octyldodecyl Oleate, Tocopherol, Cocos Nucifera (Coconut) Fruit Extract, Sodium Benzoate, Iron oxides (CI 77492), Dodecane, Hexadecane, Titanium Dioxide (CI 77891), Withania Somnifera Flower Extract, Iron Oxides (CI 77491), Vaccinium Angustifolia (Blueberry) Fruit Extract, Silica, Calcium Gluconate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Zinc Screen

100% Mineral Lotion

Broad Spectrum SPF 40 PA+++

1.7 fl. oz. / 50 ml.

BottleBottleCartonCarton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75936-223-012026-01-29C16284748780-149896155-b9c8-586f-e063-e6dba90add90Zinc Screen Broad Spectrum Sunscreen SPF 40
75936-223-022026-01-29C16284748780-149896155-b9c8-586f-e063-e6dba90add90Zinc Screen Broad Spectrum Sunscreen SPF 40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-223-01Zinc Screen Broad Spectrum Sunscreen SPF 4050 mL in 1 BOTTLELOTION506
75936-223-02Zinc Screen Broad Spectrum Sunscreen SPF 4010 mL in 1 BOTTLELOTION106

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75936-223ZINC SCREEN BROAD SPECTRUM SUNSCREEN SPF 40 (ZINC OXIDE) LOTION [SUPERGOOP, LLC]6Legacy NDC, 2 package rows20241208_87adf142-7560-30d9-e053-2a95a90aca90.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-22375936-223-01, 75936-223-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML · Source PDF

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
287a61d8-0055-6211-e063-6394a90aa3da87adf142-7560-30d9-e053-2a95a90aca902024-12-04WarningsExact identifier
spl id: 287a61d8-0055-6211-e063-6394a90aa3da
spl set id: 87adf142-7560-30d9-e053-2a95a90aca90

Reported adverse events (FAERS/openFDA)#

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