MENOKIN 30 SECONDS GLOW AND CLEAR GEL SUNSCREEN BRIGHT- avobenzone, homosalate, octisalate, octocrylene cream

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Avobenzone 2.7%

Homosalate 14.5%

Octisalate 4.5%

Octocrylene 3.0%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Helps prevent sunburn
If used as directed with other sun protection measures (see Directions) decrease the risk of skin cancer and early skin aging caused by the sun

DOSAGE & ADMINISTRATION

For sunscreen use:

Apply liberally 15 minutes before sun exposure
Reapply at least every two hours
Use a water-resistant sunscreen if swimming or sweating

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: 1) Limit time in the sun, especially from 10 a.m. to 2 p.m. 2) Wear long-sleeved shirts, pants, hats, and sunglasses

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

INACTIVE INGREDIENT

Water, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Propanediol, Glycerin, Castor Oil/IPDI Copolymer, Methyl Methacrylate Crosspolymer, Polymethylsilsesquioxane, 1,2-Hexanediol, Caprylic/Capric Triglyceride, Poly C10-30 Alkyl Acrylate, Elaeis Guineensis (Palm) Oil, Polyacrylate Crosspolymer-6, Ethylhexylglycerin, Sphingomonas Ferment Extract, Sodium Polyacryloyldimethyl Taurate, Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Adenosine, Butylene Glycol, Hydrolyzed Extensin, Niacinamide, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Acetyl Hexapeptide-8, Limnanthes Alba (Meadowfoam) Seed Oil, Panthenol, Glutathione, Ceramide NP, Hydroxyacetophenone, Ascorbic Acid, Polyurethane-15

OTHER SAFETY INFORMATION

Protect the product in the container from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MENOKIN 30 SECONDS GLOW AND CLEAR GEL SUNSCREEN BRIGHT 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87507-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	145 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	45 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	30 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	27 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
PROPANEDIOL (UNII: 5965N8W85T)
GLYCERIN (UNII: PDC6A3C0OX)
CASTOR OIL/IPDI COPOLYMER (UNII: GSA2TXZ34G)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PALM OIL (UNII: 5QUO05548Z)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DIUTAN GUM (UNII: 49VQ7E2HRT)
SODIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: NG5NG5733T)
TROMETHAMINE (UNII: 023C2WHX2V)
ADENOSINE (UNII: K72T3FS567)
NIACINAMIDE (UNII: 25X51I8RD4)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ACETYL HEXAPEPTIDE-8 AMIDE (UNII: L4EL31FWIL)
MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
PANTHENOL (UNII: WV9CM0O67Z)
GLUTATHIONE (UNII: GAN16C9B8O)
CERAMIDE NP (UNII: 4370DF050B)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87507-002-02	1 in 1 CARTON	03/31/2026
1	NDC: 87507-002-01	50 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	03/31/2026

Labeler - Forest Avenue Co., Ltd. (695547995)

Registrant - Forest Avenue Co., Ltd. (695547995)

Establishment
Name	Address	ID/FEI	Business Operations
Cit Co., Ltd.		690081646	manufacture(87507-002)