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

Open FDA National Drug Code directory

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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LAPCOS DAILY SUNSCREEN SPF 50 — United States | Molindra Medicines