Home NDC 83862-003 Florida Glow SPF 15
Product NDC 83862-003
11-digit product format 838620003
Labeler code 83862
Product ID 83862-003_5d2c4f6d-cbbf-1d14-e063-6294a90a9432
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone,Octocrylene,Octisalate
Dosage form SPRAY
Route TOPICAL
Labeler Southeast Holdings Corp.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-19
Substance AVOBENZONE; OCTOCRYLENE; OCTISALATE
Active strength 2; 1.85; 5 g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 SPF 15
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 2 g/100mL OCTOCRYLENE 1.85 g/100mL OCTISALATE 5 g/100mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83862-003-01 Florida Glow SPF 15 162 mL in 1 BOTTLE, SPRAY SPRAY 162 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83862-003 FLORIDA GLOW SPF 15 (AVOBENZONE,OCTOCRYLENE,OCTISALATE) SPRAY [SOUTHEAST HOLDINGS CORP.] 1 Current NDC, 1 package rows 20250502_56af704a-bda9-49ed-a177-a8480d90458b.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 162 of 353 · 7,041 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83862-003-01 83862000301 162 mL in 1 BOTTLE, SPRAY (83862-003-01) 162 ml 2021-01-19 No No Current