FDA.reportPublic FDA data

Mineral Sunscreen SPF 30

Manufacturer
Supergoop, LLC
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-06-03 17:51:53

Label at a glance#

ProductMineral Sunscreen SPF 30
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​Active Ingredients                                    Purpose

Zinc Oxide 12.0% ..................................... 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

INDICATIONS & USAGE SECTION

Stop use and ask a doctor is rash occurs

WARNINGS SECTION

Warnings

  • For external use only
  • Flammable: Contents under pressure. Do not punture or incinerate. Do not store at temperatures above 120 F. Do not use in the precesne of a flame or spark, or while smoking
  • Do not use on damaged or broken skin
  • When using this product keep out of eyes
  • Rinse with water to remove
  • Keep out of reach of children
  • If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

​Directions

​SHAKE WELL to activate. If the mist is clear, keep shaking.

  • Apply liberally 15 minutes before sun exposure
  • Reapply:

- after 80 minutes of swimming or sweating

- immediately after towel drying

- at least every 2 hours whem exposed to sunlight

  • Children un 6 months: Ask a doctor

​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 epsecially from 10 a.m. - 2 p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Bentonite, Butyloctyl Salicylate, Calendula Officinalis Flower Extract, Caprylhydroxamic Acid, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Seed Oil, Cetearyl Alcohol, Chamomilla Recutita (Matricaria) Flower Extract, Coco Glucoside, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Heptyl Undecylenate, Jojoba Esters, Melissa Officinalis Leaf Extract, Methyl Dihydroabietate, Nasturtium Officinale Flower/Leaf Extract, Spiraea Ulmaria Flower Extract, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Supergoop!

Play

SPF 30

100% Mineral Body Mist

with Marigold Extract

Broad Spectrum Sunscreen SPF 30

Water Resistant (80 minutes)

6 fl. oz. / 177 mL.

Principal Display PanelPrincipal Display Panel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130816218026059GTIN-13: 0816218026059
EAN-13: 0816218026059
GTIN-12: 816218026059
UPC-A: 816218026059
GTIN storage (14 digits): 00816218026059		Mineral Body Mist SPF 50.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75936-510-012026-01-09C16284748780-12cef2736-9560-d83d-e063-dadaa90ab31fMineral Sunscreen Mist SPF 30
75936-510-012026-01-09C16284748780-12cef2736-9560-d83d-e063-dadaa90ab31fMineral Sunscreen Mist SPF 30
75936-510-012025-01-30C16284748780-12cef2736-9560-d83d-e063-dadaa90ab31fMineral Sunscreen Mist SPF 30
75936-510-012025-01-30C16284748780-12cef2736-9560-d83d-e063-dadaa90ab31fMineral Sunscreen Mist SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-510-01Mineral Sunscreen SPF 30177 mL in 1 BOTTLE, SPRAYSPRAY1774

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-51075936-510-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
FILIPENDULA ULMARIA ROOT997724QNDSIACT
HEPTYL UNDECYLENATEW77QUB6GXOIACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
MELISSA OFFICINALIS LEAF50D2ZE9219IACT
METHYL DIHYDROABIETATE7666FJ0J9FIACT
NASTURTIUM OFFICINALE FLOWERING TOPW1N2U8I64GIACT
FILIPENDULA ULMARIA FLOWER06L18L32G6IACT
WATER059QF0KO0RIACT
ZINC OXIDESOI2LOH54ZACTIM
ALOE VERA LEAFZY81Z83H0XIACT
BENTONITEA3N5ZCN45CIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
SAFFLOWER OIL65UEH262ISIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CHAMOMILEFGL3685T2XIACT
COCO GLUCOSIDEICS790225BIACT
SUNFLOWER OIL3W1JG795YIIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32022-10-11full-release2026-05-31 23:50:59

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
Mineral Sunscreen SPF 30ZINC OXIDESupergoop, LLC4cf243b4-d794-401a-b209-18c7e550ef4f2026-01-09WarningsExact identifier
ndc (package): 75936-510-01
ndc (product): 75936-510
ndc11 (package): 75936051001
spl id: 47fc0e5f-df05-b716-e063-6294a90a7656
spl set id: 4cf243b4-d794-401a-b209-18c7e550ef4f

Reported adverse events (FAERS/openFDA)#

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