WONDERSCREEN BROAD SPECTRUM SPF 30- zinc oxide cream

Wonderscreen Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Wonderscreen Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by Wasatch Product Development, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Zinc Oxide

Purpose: Sunscreen

PURPOSE

Uses: Helps prevent sunburn. Higher SPF gives more sunburn protection

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

Warning:

• For External use only. Do not use on broken or damaged skin

DOSAGE & ADMINISTRATION

Directions:

• Apply liberally 15 minutes before sun or water exposure
• Immediately after towel drying
• At least every 2 hours
• Children under 6 months: ask a doctor

INACTIVE INGREDIENT

Inactive Ingredients: Water, Ethylhexyl Olivate, Dimethicone, C9-12 Alkane, Cocoglycerides, Hydroxyethyl Dimethicone Laurate, Pentylene Glycol, Butyloctyl Salicylate, Glycerin, Jojoba Esters, Pyrus Malus (Apple) Fruit Extract, Polymethylsilsesquioxane, Squalane, Dipotassium Glycyrrhizate, Beta Vulgaris (Beet) Root Extract, Fructooligosaccharides, Glycine Soja (Soybean) Seed Extract Diheptyl Succinate, Disteardimonium Hectorite, Phenoxyethanol, Sodium Chloride, Polyhydroxystearic Acid, Trihydroxystearin, Triethyl Citrate, Hydroxyacetophenone, Sodium Citrate, Tetrasodium Glutamate Diacetate, Sodium Dehydroacetate, Capryloyl Glycerin/Sebacic Acid Copolymer

PRINCIPAL DISPLAY PANEL

DIME

Wonderscreen

Broad Spectrum SPF 30

50 G

INGREDIENTS AND APPEARANCE

WONDERSCREEN BROAD SPECTRUM SPF 30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44717-062
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	19 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
DIMETHICONE 100 (UNII: RO266O364U)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
SQUALANE (UNII: GW89575KF9)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
BEET (UNII: N487KM8COK)
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
GLYCERIN (UNII: PDC6A3C0OX)
APPLE (UNII: B423VGH5S9)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
COCO-GLYCERIDES (UNII: ISE9I7DNUG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44717-062-01	50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/25/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/25/2022

Labeler - Wasatch Product Development, LLC. (962452533)