PURE SOL SPF 30 MINERAL WHIPPED SUNSCREEN (SHIMMER)- zinc oxide spray

PURE SOL SPF 30 Mineral Whipped Sunscreen (Shimmer) by

Drug Labeling and Warnings

PURE SOL SPF 30 Mineral Whipped Sunscreen (Shimmer) by is a Otc medication manufactured, distributed, or labeled by Brand 2022b LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide-15%

PURPOSE

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or
contact a Poison Control Center immediately.

WARNINGS

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

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

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURE SOL SPF 30 MINERAL WHIPPED SUNSCREEN (SHIMMER) 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84090-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
OKRA (UNII: 51ME2L7STL)
CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ISOBUTANE (UNII: BXR49TP611)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
SILVER (UNII: 3M4G523W1G)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
BUTANE (UNII: 6LV4FOR43R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GENTIANA SCABRA ROOT (UNII: GXZ33VNT92)
EDETATE DISODIUM (UNII: 7FLD91C86K)
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 64-70) (UNII: 96YYQ5TK1K)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
PROPANE (UNII: T75W9911L6)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PALMITIC ACID (UNII: 2V16EO95H1)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84090-002-01	166 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/04/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/04/2025

Labeler - Brand 2022b LLC (119190557)

Registrant - Brand 2022b LLC (119190557)