Florida Glow SPF 30

Product NDC
83862-002
11-digit product format
838620002
Labeler code
83862
Product ID
83862-002_436d52df-1e06-52c8-e063-6394a90a368a
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone,Octocrylene,Octisalate,Homosalate
Dosage form
SPRAY
Route
TOPICAL
Labeler
Southeast Holdings Corp.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-01-19
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 7; 5; 5 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Florida Glow SPF 30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100mL
HOMOSALATE7 g/100mL
OCTISALATE5 g/100mL
OCTOCRYLENE5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83862-002-01Florida Glow SPF 30162 mL in 1 BOTTLE, SPRAYSPRAY1623

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83862-002FLORIDA GLOW SPF 30 (AVOBENZONE,OCTOCRYLENE,OCTISALATE,HOMOSALATE) SPRAY [SOUTHEAST HOLDINGS CORP.]1Current NDC, 1 package rows20250502_20538bc0-10c3-492c-952a-6797e46003f2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83862-002-0183862000201162 mL in 1 BOTTLE, SPRAY (83862-002-01) 162 ml2021-01-19NoNoHistorical