SKPRADIS SUNSCREEN STICK- sunscreen stick stick

Skpradis Sunscreen Stick by

Drug Labeling and Warnings

Skpradis Sunscreen Stick by is a Otc medication manufactured, distributed, or labeled by Guangdong Miaolian Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Sunscreen

WARNINGS

For external use only

ACTIVE INGREDIENT

TOCOPHERYL ACETATE -----0.438%

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. lf swallowed, get medical help orcontact Poison Control Center right away

DOSAGE & ADMINISTRATION

Apply liberally/generously (and evenly) 15 minutes before sun exposure
For use on children less than 6 months of age, consult a health care practitioner
Reapply
At least every 2 hours
After 80 minutes of swimming or sweating
Immediately after towel drying

INDICATIONS & USAGE

Helps prevent sunbum.
lf used as directed with other sun protectionmeasures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

INACTIVE INGREDIENT

ETHYLHEXYL PALMITATE
MICROCRYSTALLINE WAX
CAPRYLIC/CAPRIC TRIGLYCERIDE
OZOKERITE
ETHYLHEXYL SALICYLATE
SYNTHETIC WAX
DICAPRYLYL CARBONATE
DIETHYLHEXYL BUTAMIDO TRIAZONE
BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE
ISODODECANE
ETHYLHEXYL METHOXYCINNAMATE
BHT
OCTOCRYLENE
Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer
SILICA DIMETHYL SILYLATE
FRAGRANCE
TRIDECYL TRIMELLITATE
CI 19140
WATER
BUTYLENE GLYCOL
ALOE BARBADENSIS LEAF EXTRACT
PHENOXYETHANOL
WATER
CAPRYLYL GLYCOL
ACETYL HEXAPEPTIDE-8
COPPER TRIPEPTIDE-1
NIACINAMIDE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SKPRADIS SUNSCREEN STICK 
sunscreen stick stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84507-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1)	.ALPHA.-TOCOPHEROL	0.438 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51)
OCTOCRYLENE (UNII: 5A68WGF6WM)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
NIACINAMIDE (UNII: 25X51I8RD4)
CERESIN (UNII: Q1LS2UJO3A)
SYNTHETIC WAX (540 MW) (UNII: DW2TC44JRY)
BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE (UNII: PWZ1720CBH)
ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
DIETHYLHEXYL BUTAMIDO TRIAZONE (UNII: 2UTZ0QC864)
CI 19140 (UNII: I753WB2F1M)
ETHYLHEXYL SALICYLATE (UNII: 4X49Y0596W)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
COPPER TRIPEPTIDE-1 (UNII: 6BJQ43T1I9)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ISODODECANE (UNII: A8289P68Y2)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
BHT (UNII: 1P9D0Z171K)
FRAGRANCE LEMON ORC2001060 (UNII: K1725A7G95)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Product Characteristics
Color	yellow (faint yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84507-036-01	20 g in 1 BOX; Type 0: Not a Combination Product	03/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/31/2025

Labeler - Guangdong Miaolian Cosmetics Co., Ltd. (707598469)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Miaolian Cosmetics Co., Ltd.		707598469	manufacture(84507-036) , label(84507-036)