LAPCOS DAILY SUNSCREEN SPF 50

Product NDC
85586-001
11-digit product format
855860001
Labeler code
85586
Product ID
85586-001_341c720c-38dd-4cba-e063-6394a90a66a8
Type
HUMAN OTC DRUG
Nonproprietary name
sunscreen
Dosage form
CREAM
Route
TOPICAL
Labeler
LAP USA, INC.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-04-23
Substance
ETHYLHEXYL SALICYLATE; HOMOSALATE; OCTOCRYLENE; ZINC OXIDE
Active strength
4.5; 6; 5; 10.3 g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
LAPCOS DAILY SUNSCREEN SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ETHYLHEXYL SALICYLATE4.5 g/100g
HOMOSALATE6 g/100g
OCTOCRYLENE5 g/100g
ZINC OXIDE10.3 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4X49Y0596W, V06SV4M95S, 5A68WGF6WM, SOI2LOH54Z

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85586-001-01LAPCOS DAILY SUNSCREEN SPF 5050 g in 1 TUBECREAM502
85586-001-02LAPCOS DAILY SUNSCREEN SPF 501 in 1 BOXCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85586-001LAPCOS DAILY SUNSCREEN SPF 50 (SUNSCREEN) CREAM [LAP USA, INC.]2Current NDC, 2 package rows20250503_337c3528-5739-6b4a-e063-6294a90a3cb4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85586-001-018558600010150 g in 1 TUBE50 gHistorical
85586-001-02855860001021 TUBE in 1 BOX (85586-001-02) / 50 g in 1 TUBE (85586-001-01) 1 tube2025-04-23NoNoCurrent