United States · FDA National Drug Code directory
LAPCOS DAILY SUNSCREEN SPF 50
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 85586-001_341c720c-38dd-4cba-e063-6394a90a66a8
- Product NDC
- 85586-001
- Form
- CREAM
- Composition / generic term
- sunscreen
- Labeler
- LAP USA, INC.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250423
- Source listing expiry
- 20261231
Source-listed ingredients
- ETHYLHEXYL SALICYLATE — 4.5 g/100g
- OCTOCRYLENE — 5 g/100g
- HOMOSALATE — 6 g/100g
- ZINC OXIDE — 10.3 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 BOX (85586-001-02) / 50 g in 1 TUBE (85586-001-01) · 85586-001-02
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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