SHEGLAM DEW AND DONE SKIN TINT WITH SPF 20 DARK CLOVE- zinc oxide cream

Sheglam Dew and Done Skin Tint with SPF 20 Dark Clove by

Drug Labeling and Warnings

Sheglam Dew and Done Skin Tint with SPF 20 Dark Clove by is a Otc medication manufactured, distributed, or labeled by EVER FAME PTE. LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Zinc Oxide 14.625%

Purpose

Sunscreen

Use

• helps prevent sunburn

Warnings

Skin Cancer/Skin Aging Alert:Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. 

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.

Directions

• apply liberally 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating 
• children under 6 months of age: Ask a doctor

Other information

• protect the product in this container from excessive heat and direct sun

Inactive ingredients

Water, Glycerin, Dimethicone, Caprylyl Methicone, C9-12 Alkane, Butylene Glycol, Butyloctyl Salicylate, Dimethicone/PEG-10/15 Crosspolymer, Trimethylsiloxysilicate, Jojoba Seed Oil, Oryzanol, Isononyl Isononanoate, Magnesium Sulfate, 1,2-Hexanediol, PEG-10 Dimethicone, Hydroxyacetophenone, Triethoxycaprylylsilane, Sodium Hyaluronate, Dipropylene Glycol, Sodium Citrate, Gotu Kola Leaf Extract, Bisabolol, Tocopherol, Snow Lotus Extract, Xylitylglucoside, Anhydroxylitol, Xylitol, Ethylhexylglycerin, Ginger Root Extract, Titanium Dioxide Color, Iron Oxides Color.

Package Labeling:

INGREDIENTS AND APPEARANCE

SHEGLAM DEW AND DONE SKIN TINT WITH SPF 20 DARK CLOVE 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85068-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	146.25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
C9-12 ALKANE (UNII: 7J5R5W72QM)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)
JOJOBA OIL (UNII: 724GKU717M)
ORYZANOL (UNII: SST9XCL51M)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
MAGNESIUM SULFATE (UNII: DE08037SAB)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
BISABOLOL (UNII: 24WE03BX2T)
TOCOPHEROL (UNII: R0ZB2556P8)
XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
ANHYDROXYLITOL (UNII: 8XWR7NN42F)
XYLITOL (UNII: VCQ006KQ1E)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GINGER (UNII: C5529G5JPQ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85068-012-01	1 in 1 CARTON	05/30/2025
1		30 mL in 1 TUBE; 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	05/30/2025

Labeler - EVER FAME PTE. LTD. (659974769)