United States · FDA National Drug Code directory

Florida Glow 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
83862-001_436d3b8f-55c5-c8a4-e063-6294a90a37f9
Product NDC
83862-001
Form
SPRAY
Composition / generic term
Avobenzone,Octocrylene,Octisalate,Homosalate
Labeler
Southeast Holdings Corp.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20210119
Source listing expiry
20261231

Source-listed ingredients

  • AVOBENZONE — 3 g/100mL
  • OCTOCRYLENE — 5 g/100mL
  • OCTISALATE — 5 g/100mL
  • HOMOSALATE — 10 g/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 162 mL in 1 BOTTLE, SPRAY (83862-001-01) · 83862-001-01

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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Florida Glow SPF 50 — United States | Molindra Medicines