SKY AND SOL SUNSCREEN SPF 50- zinc oxide cream

Sky and Sol Sunscreen SPF 50 by

Drug Labeling and Warnings

Sky and Sol Sunscreen SPF 50 by is a Otc medication manufactured, distributed, or labeled by Delta Ecommerce LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Sunscreen

INDICATIONS & USAGE

helps prevent sunburn; if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

DOSAGE & ADMINISTRATION

Shake well before use.
Apply liberally 15 minutes before sun exposure.
Reapply:
after 80 minutes of swimming or sweating
immediately after towel drying
at least every 2 hours

INACTIVE INGREDIENT

Aqua (Water), Tallow, Simmondsia Chinensis (Jojoba) Seed Oil, Jojoba Esters, Lecithin, Cera Alba (Beeswax), Silica, Tocopherol (Vitamin E), Leuconostoc/Radish Root Ferment Filtrate

WARNINGS

Warnings:
For external use only.
Do not use on damaged or broken skin.
Stop use and ask a doctor if rash occurs.
When using this product, keep out of eyes. Rinse with water to remove.

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SKY AND SOL SUNSCREEN SPF 50 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84632-0503
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	25 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
JOJOBA OIL (UNII: 724GKU717M)
HYDROLYZED JOJOBA ESTERS (UNII: UDR641JW8W)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TALLOW (UNII: 98HPY76U4W)
WATER (UNII: 059QF0KO0R)
BEESWAX (UNII: 2ZA36H0S2V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84632-0503-3	1 g in 1 TUBE; Type 0: Not a Combination Product	01/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/29/2025

Labeler - Delta Ecommerce LLC (118430341)