LAPCOS FRESH DAILY SUN- octinoxate, octisalate cream

LAPCOS Fresh Daily Sun by

Drug Labeling and Warnings

LAPCOS Fresh Daily Sun by is a Otc medication manufactured, distributed, or labeled by LAP CO.,LTD, Cosmax, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Ethylhexyl Methoxycinnamate 7.0%, Ethylhexyl Salicylate 4.5%

INACTIVE INGREDIENT

Inactive ingredients: Water,Glycerin,Dicaprylyl Carbonate,Butyl Methoxydibenzoylmethane,Alcohol Denat.,Aloe Barbadensis Leaf Water,Water,Calendula Officinalis Flower Extract,Gentiana Lutea Root Extract,Achillea Millefolium Extract,Artemisia Absinthium Extract,Arnica Montana Flower Extract,Silica,Glyceryl Stearate,PEG-100 Stearate,Triceteareth-4 Phosphate,Glycol Stearate,PEG-2 Stearate,Glyceryl Caprylate,Tromethamine,Polyacrylate-13,Caprylyl Glycol,Polyisobutene,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Polysorbate 20,Caprylic/Capric Triglyceride,Lecithin,Cetearyl Alcohol,Carbomer,Alcohol,Disodium EDTA,Phenoxyethanol,Potassium Sorbate,Fragrance(Parfum)

PURPOSE

Purpose: Sunscreen

WARNINGS

Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Keep Out of Reach of Children

DESCRIPTION

Uses: - Helps prevent sunburn - Higher SPF gives more sun protection

Directions: - Apply generously and as needed. - Children under 6 months of age : Ask a doctor. - Reapply as needed or after towel drying, swimming or sweating.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LAPCOS FRESH DAILY SUN 
octinoxate, octisalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71379-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	Octinoxate	3.50 g  in 50 mL
Octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	Octisalate	2.25 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71379-010-02	1 in 1 CARTON	04/01/2017
1	NDC: 71379-010-01	50 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/01/2017

Labeler - LAP CO.,LTD (689041115)

Registrant - LAP CO.,LTD (689041115)

Establishment
Name	Address	ID/FEI	Business Operations
LAP CO.,LTD		689041115	relabel(71379-010)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc		689049693	manufacture(71379-010)