FDA.reportPublic FDA data

84090-002-01.PURE SOL SPF 30 Mineral Whipped Sunscreen(Shimmer)- Spray 166ml

Manufacturer
Brand 2022b LLC
Effective date
2025-10-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:15:55

Label at a glance#

ProductPURE SOL SPF 30 Mineral Whipped Sunscreen (Shimmer)
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide-15%

OTC - PURPOSE SECTION

helps prevent sunburn • higher SPF gives more sunburn - protection • helps protect the skin against the harmful effects of - UVA and UVB rays

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 immediately.

WARNINGS SECTION

For external use only

When using this product

avoid contact with the eyes. If contact
occurs rinse thoroughly with water.

Stop use and ask a doctor if

rash or irritation develops and lasts.

INDICATIONS & USAGE SECTION

apply generously and evenly to all exposed areas before sun
exposure • reapply as needed or after towel drying, swimming,
perspiring or vigorous activity • children under 6 months of age:
ask a doctor

INACTIVE INGREDIENT SECTION

Water (Aqua)
Butane
Isobutane
Propane
Glycerin
PEG-17 Dimethicone
Propylene Glycol
Stearic Acid
Palmitic Acid
Triethanolamine
Glyceryl Stearate
PEG-100 Stearate
PEG-7 Glyceryl Cocoate
Jojoba Wax PEG-120 Esters
Cetearyl Alcohol
Hydroxyacetophenone
1,2-Hexanediol
Butylene Glycol
Gentiana Scabra Root Extract
Dipotassium Glycyrrhizate
Calcium SodiumBorosilicate
Silver
Sodium Hyaluronate
Disodium EDTA
Hibiscus Esculentus Fruit Extract

DOSAGE & ADMINISTRATION SECTION

Apply generously and evenly over whole body 20 minutes before sun exposure. Reapply frequently.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84090-002-01PURE SOL SPF 30 Mineral Whipped Sunscreen (Shimmer)166 mL in 1 BOTTLESPRAY1661

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84090-00284090-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
STEARIC ACID4ELV7Z65APIACT
TRIETHANOLAMINE9O3K93S3TKIACT
OKRA51ME2L7STLIACT
CALCIUM SODIUM BOROSILICATE4MM76N4WMYIACT
HYALURONATE SODIUMYSE9PPT4THIACT
ISOBUTANEBXR49TP611IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
SILVER3M4G523W1GIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
BUTANE6LV4FOR43RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GENTIANA SCABRA ROOTGXZ33VNT92IACT
EDETATE DISODIUM7FLD91C86KIACT
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 64-70)96YYQ5TK1KIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
ZINC OXIDESOI2LOH54ZACTIB
DIPOTASSIUM GLYCYRRHIZATECA2Y0FE3FXIACT
PROPANET75W9911L6IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PALMITIC ACID2V16EO95H1IACT
PEG-12 DIMETHICONEZEL54N6W95IACT

Source Document#

Source XML

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
PURE SOL SPF 30 Mineral Whipped Sunscreen (Shimmer)ZINC OXIDEBrand 2022b LLC4051ced5-85cf-6211-e063-6394a90a09fc2025-10-04WarningsExact identifier
ndc (package): 84090-002-01
ndc (product): 84090-002
ndc11 (package): 84090000201
spl id: 4051ced5-85d0-6211-e063-6394a90a09fc
spl set id: 4051ced5-85cf-6211-e063-6394a90a09fc

Reported adverse events (FAERS/openFDA)#

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