EVEREDEN KIDS COOLING MINERAL SUNSTICK SPF30- zinc oxide stick

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 11.5%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Uses:

• Helps prevent sunburn

WARNINGS

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.

Stop use and ask a doctor if rash occurs.

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

DOSAGE & ADMINISTRATION

Directions:

• Apply liberally 15 minutes before sun exposure.
• Reapply at least every 2 hours.
• Use a water-resistant susncreen if swimming or sweating.
• Children under 6 months of age: Ask a doctor.
• Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early aging skin. To decrease this risk, regularly use a sunscreen with broad spectrum SPF value of 15 or higher and other sun protection measures. including:
  • Limit your time in the sun, especially between 10 a.m. - 2 p.m.
  • Wear long-sleeved shirts, pants, hats, sunglasses.

INACTIVE INGREDIENT

Dicaprylyl Carbonate, Octyldodecanol, Water (Aqua), Caprylic/Capric Triglyceride, Silica, Dibutyl Lauroyl Glutamide, Dextrin Palmitate, Dibutyl Ethylhexanoyl Glutamide, 1,2-Hexanediol, Butylene Glycol, Polyglyceryl-10 Behenate/Eicosadioate, Propanediol, Sodium Chloride, Polyhydroxystearic Acid, Jojoba Esters, Bisabolol, Ethyl Ferulate, Pongamia Pinnata Seed Extract, Magnolia Officinalis Bark Extract, Tocopheryl Acetate, Chimyl Alcohol, Sodium Phytate, Glycerin, Tocopherol, Naringin

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EVEREDEN KIDS COOLING MINERAL SUNSTICK SPF30 
zinc oxide stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72113-116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	115 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PROPANEDIOL (UNII: 5965N8W85T)
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
BISABOLOL (UNII: 24WE03BX2T)
DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR)
PONGAMIA PINNATA SEED (UNII: C2BRV53B1V)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYL FERULATE (UNII: 5B8915UELW)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
NARINGIN (UNII: N7TD9J649B)
CHIMYL ALCOHOL (UNII: UJ10V6YY6H)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
TOCOPHEROL (UNII: R0ZB2556P8)
HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
SODIUM PHYTATE (UNII: 88496G1ERL)
OCTYLDODECANOL (UNII: 461N1O614Y)
DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72113-116-22	1 in 1 CARTON	05/18/2026
1		15.5 g in 1 CANISTER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/18/2026

Labeler - Eden Brands Inc. (081062339)