FDA.reportPublic FDA data

100% Mineral Lotion Broad Spectrum Sunscreen SPF 50 with Green Algae

Manufacturer
Supergoop LLC
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
monthly-update
Hydrated at
2026-06-03 17:52:19

Label at a glance#

Product100% Mineral Broad Spectrum Sunscreen SPF 50
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

TItanium Dioxide 2.3% Sunscreen

Zinc Oxide 17.9% 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

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply generously and evenly 15 minutes before sun exposure

reapply

  • after80 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 sub 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 Arachidyl Alcohol, Arachidyl Glucoside, Astrocaryum Vulgare Kernel Oil, Behenyl Alcohol, Bisabolol, Butyloctyl Salicylate, C13-14 Alkane, Caprylhydroxamic Acid, Caprylic/Capric Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Caprylyl Glycol, Cellulose Gum, Cetearyl Alcohol, Cetyl Alcohol, Citric Acid, Coco-Glucosde, Diheptyl Succinate, Erythritol, Ethyl Ferulate, Glycerin, Haematococcus Pluvialis Extract, Jojoba Esters, Lauryl Laurate, Methyl dihydroabietate, Microcrystalline Cellulose, Neopentyl Glycol Diheptanoate, Polyester-7, Polyester-8, Polyhydroxystearic Acid, Propanediol, Sea Water, Sodium Gluconate, Sodium Stearoyl Glutamate, Tocopherol, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Supergoop!

PLAY

SPF 50

100% Mineral Lotion

With Green Algae

Broad Spectrum Sunscreen SPF 50 PA++++

Water resistant (80 minutes)

3.4 fl. oz. / 100 ml.

Play 100% mineral lotion tubePlay 100% mineral lotion tube

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130816218029838GTIN-13: 0816218029838
EAN-13: 0816218029838
GTIN-12: 816218029838
UPC-A: 816218029838
GTIN storage (14 digits): 00816218029838		PLAY 100 Mineral Lotion SPF 50_100ml_TUBE.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-362-01100% Mineral Broad Spectrum Sunscreen SPF 5030 mL in 1 TUBELOTION305
75936-362-02100% Mineral Broad Spectrum Sunscreen SPF 50100 mL in 1 TUBELOTION1005

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-36275936-362-01, 75936-362-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
DOCOSANOL9G1OE216XYIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
SODIUM GLUCONATER6Q3791S76IACT
COCO GLUCOSIDEICS790225BIACT
ETHYL FERULATE5B8915UELWIACT
HAEMATOCOCCUS PLUVIALIS31T0FF0472IACT
METHYL DIHYDROABIETATE7666FJ0J9FIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
POLYESTER-70841698D2FIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
PROPANEDIOL5965N8W85TIACT
SODIUM CHLORIDE451W47IQ8XIACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
TOCOPHEROLR0ZB2556P8IACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
DIHEPTYL SUCCINATE057N7SS26YIACT
CETYL ALCOHOL936JST6JCNIACT
GLYCERINPDC6A3C0OXIACT
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED)T9296U138PIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
ASTROCARYUM VULGARE KERNEL OIL1IQY04O559IACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
LEVOMENOL24WE03BX2TIACT
ERYTHRITOLRA96B954X6IACT
LAURYL LAURATEGPW77G0937IACT
CAPRYLYL GLYCOL00YIU5438UIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-12-05full-release2026-06-01 00:41:09

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
100% Mineral Broad Spectrum Sunscreen SPF 50TITANIUM DIOXIDE, ZINC OXIDESupergoop LLCd6fcc065-cbcd-0b81-e053-2a95a90ab1f92026-01-09WarningsExact identifier
ndc (package): 75936-362-02
ndc (package): 75936-362-01
ndc (product): 75936-362
ndc11 (package): 75936036202
ndc11 (package): 75936036201
spl id: 47fbec0a-e071-4815-e063-6394a90aa104
spl set id: d6fcc065-cbcd-0b81-e053-2a95a90ab1f9

Reported adverse events (FAERS/openFDA)#

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