Sky and Sol Face Sunscreen SPF 50 by Delta Ecommerce LLC

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]

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

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Sunscreen

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

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

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 product is swallowed, get
medical help or contact a Poison Control Center right away.

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

Packaging

SKY AND SOL FACE SUNSCREEN SPF 50 
non-nano zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 84632-5050
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE25 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
HYDROLYZED JOJOBA ESTERS (UNII: UDR641JW8W)  
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
TALLOW (UNII: 98HPY76U4W)  
BEESWAX (UNII: 2ZA36H0S2V)  
WATER (UNII: 059QF0KO0R)  
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)  
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 84632-5050-385 g in 1 TUBE; Type 0: Not a Combination Product01/04/202503/31/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/04/202503/31/2025
Labeler - Delta Ecommerce LLC (118430341)

Revised: 4/2026
 

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