SKY AND SOL FACE SUNSCREEN SPF 50- non-nano zinc oxide cream

Sky and Sol Face Sunscreen SPF 50 by

Drug Labeling and Warnings

Sky and Sol Face 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

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

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

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

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SKY AND SOL FACE SUNSCREEN SPF 50 
non-nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84632-5050
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
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
HYDROLYZED JOJOBA ESTERS (UNII: UDR641JW8W)
TALLOW (UNII: 98HPY76U4W)
BEESWAX (UNII: 2ZA36H0S2V)
WATER (UNII: 059QF0KO0R)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84632-5050-3	85 g in 1 TUBE; Type 0: Not a Combination Product	01/04/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/04/2025

Labeler - Delta Ecommerce LLC (118430341)