PURE SOL SPF 30 MINERAL WHIPPED SUNSCREEN- zinc oxide spray

PURE SOL SPF 30 Mineral Whipped Sunscreen by

Drug Labeling and Warnings

PURE SOL SPF 30 Mineral Whipped Sunscreen 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（nano） 15%

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

PURPOSE

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

WARNINGS

For external use only

When using this product

Avoid contact with the eyes. If contact occurs
rinse thoroughly with water
do not puncture or incinerate. Contents under pressure. Do not store at
temperatures above 120°F

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
do not spray directly on face. Spray into hands and apply to face
use in well-ventilated areas

INACTIVE INGREDIENT

Water
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
Sodium Hyaluronate
Disodium EDTA
Hibiscus Esculentus Fruit Extract

DOSAGE & ADMINISTRATION

Apply tiberally 15 minutes before sun exposure.
Reapoly. at least every 2 hours or after 80 minutes of swimming or sweating.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURE SOL SPF 30 MINERAL WHIPPED SUNSCREEN 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84090-003
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
PROPANE (UNII: T75W9911L6)
STEARIC ACID (UNII: 4ELV7Z65AP)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
WATER (UNII: 059QF0KO0R)
GENTIANA SCABRA ROOT (UNII: GXZ33VNT92)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
PALMITIC ACID (UNII: 2V16EO95H1)
PEG-100 STEARATE (UNII: YD01N1999R)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 64-70) (UNII: 96YYQ5TK1K)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ISOBUTANE (UNII: BXR49TP611)
BUTANE (UNII: 6LV4FOR43R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
OKRA (UNII: 51ME2L7STL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84090-003-01	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)