SUNSCREEN STICK- homosalate 15%, octisallate 5%, ensulizole 4% stick

Sunscreen Stick by

Drug Labeling and Warnings

Sunscreen Stick by is a Otc medication manufactured, distributed, or labeled by Foshan Sugar Max Cosmetics CO.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Homosalate 15%,0ctisalate 5%,Ensulizole 4%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Uses helps prevent sunbum 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 externall use only.

DO NOT USE

Do not use on damaged or broken skin.

WHEN USING

When using this product keep out of eyes. Rinse with water to remove.

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out ofreach ofchildren. lf product is swallowed, get medical help or contact a Poison Control Center right away.
May stain some fabrics.

DOSAGE & ADMINISTRATION

Directions apply liberally 15 minutes before sun exposure m reapply: after 80 minutes of swimming or sweating lmmediately after towel drying -at least every 2 hours Sun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including. limit time in the sun,especially from 10 a.m.-2 p.m. wearlong-sleeved shirts, pants, hats, and sunglasses
children under 6 months: Ask a doctor

INACTIVE INGREDIENT

C12‑15 Alkyl Benzoate
Caprylic/Capric Triglyceride
Isododecane
Neopentyl Glycol Diheptanoate
VP/Hexadecene Copolymer
Beeswax
Candelilla Wax
Microcrystalline Wax
Tocopherol (Vitamin E)
Caprylyl Glycol
Phenylpropanol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUNSCREEN STICK 
homosalate 15%, octisallate 5%, ensulizole 4% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84938-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.06 g  in 1 g
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	0.05 g  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	0.15 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
BEESWAX (UNII: 2ZA36H0S2V)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
PHENYLPROPANOL (UNII: 0F897O3O4M)
VP/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
CANDELILLA WAX (UNII: WL0328HX19)
ISODODECANE (UNII: A8289P68Y2)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84938-015-01	75 g in 1 BOTTLE; Type 0: Not a Combination Product	12/18/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/18/2025

Labeler - Foshan Sugar Max Cosmetics CO.,Ltd (700689935)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan Sugar Max Cosmetics CO.,Ltd		700689935	manufacture(84938-015)