FDA.reportPublic FDA data

(Re) Setting 100% mineral Powder Light Broad Spectrum SPF 35

Manufacturer
Supergoop, LLC | Port Jervis Laboratories, Inc
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
monthly-update
Hydrated at
2026-06-03 17:52:10

Label at a glance#

Product(Re) Setting 100% mineral Powder Light Broad Spectrum SPF 35
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 24.7% Purpose Sunscreen

OTC - PURPOSE SECTION

Sunscreen

  • 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 swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

Stop use and ask a Doctor if rash occurs.

WARNINGS SECTION

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.

DOSAGE & ADMINISTRATION SECTION

  • apply generously and evenly 15 minutes before sun exposure
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating
  • 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 10 a.m. - 2 p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses
  • Children under 6 months: Ask a doctor.

INACTIVE INGREDIENT SECTION

Calcium Aluminum Borosilicate, Silica, Trimethylsiloxysilicate, Calcium Sodium Borosilicate, Polymethyl Methacrylate, Lauroyl Lysine, Polyglyceryl-10 Pentaisostearate, Boron Nitride, Triethoxycaprylysilane, Ethylhexylglycerin, Nylon-6/12, Sodium Dehydroacetate, Olive Glycerides, Ascorbyl Palmitate, Ceramide 3, Iron OXides (CI 77492, 77491, 77499)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Supergoop!

(RE) SETTING

100% MINERAL POWDER

SPF 35

Light

Broad Spectrum Sunscreen

SPF 35 PA+++

0.15 oz./4.25 g

SPF 35 LightSPF 35 Light

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130816218023027GTIN-13: 0816218023027
EAN-13: 0816218023027
GTIN-12: 816218023027
UPC-A: 816218023027
GTIN storage (14 digits): 00816218023027		Re setting 100 Mineral Powder SPF 35 LIGHT_CART9.1.20a.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-166-01(Re) Setting 100% mineral Powder Light Broad Spectrum SPF 354.25 g in 1 BOTTLEPOWDER4.256
75936-166-02(Re) Setting 100% mineral Powder Light Broad Spectrum SPF 354.25 g in 1 JARPOWDER4.256

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-16675936-166-01, 75936-166-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
ASCORBYL PALMITATEQN83US2B0NIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
POLY(METHYL METHACRYLATE; 450000 MW)Z47NNT4J11IACT
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8)5041RX63GNIACT
LAUROYL LYSINE113171Q70BIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
CALCIUM ALUMINUM BOROSILICATE3JRB8A35M0IACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
CERAMIDE 34370DF050BIACT
BORON NITRIDE2U4T60A6YDIACT
SODIUM DEHYDROACETATE8W46YN971GIACT
ZINC OXIDESOI2LOH54ZACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-12-04full-release2026-06-01 00:40:38

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
(Re) Setting 100% mineral Powder Light Broad Spectrum SPF 35ZINC OXIDESupergoop, LLCaed5a7ef-5cf2-6738-e053-2a95a90aa7f72026-01-09WarningsExact identifier
ndc (package): 75936-166-02
ndc (package): 75936-166-01
ndc (product): 75936-166
ndc11 (package): 75936016601
ndc11 (package): 75936016602
spl id: 47f8a103-8ed0-6eff-e063-6394a90a1aaf
spl set id: aed5a7ef-5cf2-6738-e053-2a95a90aa7f7

Reported adverse events (FAERS/openFDA)#

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