LAPCOS DAILY SUNSCREEN SPF 50- sunscreen cream

LAPCOS DAILY SUNSCREEN SPF 50 by

Drug Labeling and Warnings

LAPCOS DAILY SUNSCREEN SPF 50 by is a Otc medication manufactured, distributed, or labeled by LAP USA, INC., COSMAX, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients Purpose
Homosalate 6.0% Sunscreen
Octisalate 4.5% Sunscreen
Octocrylene 5.0% Sunscreen
Zinc Oxide 10.3% Sunscreen

INDICATIONS & USAGE

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.

WARNINGS

For external use only.

DO NOT USE

on damaged or broken skin

WHEN USING

Avoid contact with eyes. Rinse thoroughly with water if contact occurs.

STOP USE

rash occurs.

KEEP OUT OF REACH OF CHILDREN

If swallowed, seek medical assistance or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hour. 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: Limit time in the sun, especially from 10 a.m. - 2 p.m. Wear long-sleeved shirts, pants, hats, and sunglasses. For children under 6 months of age, consult a doctor.

STORAGE AND HANDLING

Protect this product from excessive heat, freezing and direct sunlight. Store at room temperature.
May cause staining on some fabrics.

INACTIVE INGREDIENT

Water, Caprylic/Capric Triglyceride, Propanediol, Glycerin, Coco-Caprylate/Caprate, Cetearyl Olivate, 1,2-Hexanediol, Pentylene Glycol, Potassium Cetyl Phosphate, Sorbitan Olivate, Cetearyl Alcohol, Glyceryl Stearate, Lauroyl Lysine, Hydroxyacetophenone, Sodium Acrylates Crosspolymer-2, Triethoxycaprylylsilane, Sodium Polyacryloyldimethyl Taurate, Stearic Acid, Panthenol, Tromethamine, Neopentyl Glycol Diethylhexanoate, Trisodium Ethylenediamine Disuccinate, Butylene Glycol, Polyacrylate Crosspolymer-6, Panax Ginseng Berry Extract, Panax Ginseng Extract, Panax Ginseng Leaf/Stem Extract, Panax Ginseng Root Extract, Acetyl Glucosamine, Sodium Hyaluronate, Ethylhexylglycerin, Maltodextrin, Schisandra Sphenanthera Fruit Extract, Caprylyl Glycol, Glycyrrhiza Uralensis (Licorice) Root Extract, Dipropylene Glycol, Nelumbo Nucifera Flower Extract, Cimicifuga Racemosa Root Extract, Resveratrol, Silybum Marianum Extract, Dimethylsilanol Hyaluronate, Hyaluronic Acid, Sodium Acetylated Hyaluronate, BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW), PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER

Purpose

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.

PRINCIPAL DISPLAY PANEL

LAPCOS
SPF 50
BROAD SPECTRUM
DAILY SUNSCREEN HYBRID FORMULA
with Ginseng Extract
50 g / 1.76 OZ.

INGREDIENTS AND APPEARANCE

LAPCOS DAILY SUNSCREEN SPF 50 
sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85586-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ETHYLHEXYL SALICYLATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	ETHYLHEXYL SALICYLATE	4.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LAUROYL LYSINE (UNII: 113171Q70B)
HYALURONIC ACID (UNII: S270N0TRQY)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
PANAX GINSENG WHOLE (UNII: 9L5JEP7MES)
RESVERATROL (UNII: Q369O8926L)
PROPANEDIOL (UNII: 5965N8W85T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
PANAX GINSENG FRUIT (UNII: E35T4MOI3E)
PANAX GINSENG LEAF (UNII: F055A23N6X)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SILYBUM MARIANUM WHOLE (UNII: JLK089424F)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SODIUM ACRYLATES CROSSPOLYMER-2 (UNII: D3HPR4WW6F)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PANAX GINSENG ROOT (UNII: CUQ3A77YXI)
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
SODIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: NG5NG5733T)
NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
CIMICIFUGA RACEMOSA ROOT (UNII: K73E24S6X9)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PANTHENOL (UNII: WV9CM0O67Z)
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
ACETYL GLUCOSAMINE (UNII: V956696549)
POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)
SORBITAN OLIVATE (UNII: MDL271E3GR)
SCHISANDRA SPHENANTHERA FRUIT (UNII: 13I1E39KYV)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
TROMETHAMINE (UNII: 023C2WHX2V)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
STEARIC ACID (UNII: 4ELV7Z65AP)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85586-001-02	1 in 1 BOX	04/23/2025
1	NDC: 85586-001-01	50 g 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	04/23/2025

Labeler - LAP USA, INC. (085477539)

Registrant - LAP USA, INC. (085477539)

Establishment
Name	Address	ID/FEI	Business Operations
COSMAX, INC.		689049693	manufacture(85586-001)