Home NDC 83862-004 Florida Glow face shield SPF 55
Product NDC 83862-004
11-digit product format 838620004
Labeler code 83862
Product ID 83862-004_436d63df-c613-02a6-e063-6294a90a7fd3
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octocrylene, Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Southeast Holdings Corp.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-19
Substance HOMOSALATE; OCTOCRYLENE; ZINC OXIDE
Active strength 10; 5; 5.8 g/100mL; g/100mL; g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Florida Glow face shield SPF 55
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 10 g/100mL OCTOCRYLENE 5 g/100mL ZINC OXIDE 5.8 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup 5A68WGF6WM Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83862-004-01 Florida Glow face shield SPF 55 70 mL in 1 BOTTLE LOTION 70 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83862-004 FLORIDA GLOW FACE SHIELD SPF 55 (HOMOSALATE, OCTOCRYLENE, ZINC OXIDE) LOTION [SOUTHEAST HOLDINGS CORP.] 1 Current NDC, 1 package rows 20250502_cea54600-5308-4b9f-98ca-fef0b26d79c1.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83862-004-01 83862000401 70 mL in 1 BOTTLE (83862-004-01) 70 ml 2021-01-19 No No Current