Active Ingredients

Manufacturer
Southeast Holdings Corp. | Southeast Holdings Corp
Effective date
2026-10-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-10-24 01:01:12

Label at a glance#

ProductFlorida Glow SPF 15
Active ingredientAVOBENZONE, OCTOCRYLENE, OCTISALATE
Label structure9 sections

Indications and uses

Helps prevent sunburn If used as directed with other sun protection measures ( see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

Apply liberally 15 minutes before sun exposure • Reapply: • After 80 minutes of swimming or sweating • Immediately after towel drying • at least every 2 hours. • Children under 6 months: Ask a doctor. Sun Protection Measures . Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with Broad Spectrum of 15 or nigher and other sun protectio...

Label contents#

Full prescribing information#

Active Ingredients                    

OTC - ACTIVE INGREDIENT SECTION

Octisalate 5%                          
Octocrylene 1.85%
Avobenzone 2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn
  • If used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

Stop use and ask a doctorif rash occurs.

Do not useon damaged or broken skin.

When using this productKeep out of eyes.Rinse with water to remove.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure
• Reapply:
• After 80 minutes of swimming or sweating
• Immediately after towel drying
• at least every 2 hours.
• Children under 6 months: Ask a doctor.
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with Broad Spectrum of 15 or nigher and other sun protection measures, including:
• limit time in the sun, espec1ally from 10 a.m.- 2 p.m.
• wear long sleeve shirts, pants, hats & sunglasses

Inactive Ingredients

INACTIVE INGREDIENT SECTION

SD Alcohol 40-B, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Fragrance, Coconut Oil, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1 , Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Glycerin, Water, Carbomer, Butylene Glycol, Polysorbate 20

Other Information

SPL UNCLASSIFIED SECTION

• protect this product from heat and direct sun.
• may stain or damage some fabrics or surfaces.

SPL UNCLASSIFIED SECTION

Questions or Comments?
Call 1 (561) 503-6592

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BOV canBOV can

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83862-00383862-003-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-11-12full-release2026-06-01 01:43:34
12025-04-30full-release2026-06-01 01:00:09

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Florida Glow SPF 15AVOBENZONE,OCTOCRYLENE,OCTISALATESoutheast Holdings Corp.56af704a-bda9-49ed-a177-a8480d90458b2025-11-12WarningsExact identifier
ndc (package): 83862-003-01
ndc (product): 83862-003
ndc11 (package): 83862000301
spl set id: 56af704a-bda9-49ed-a177-a8480d90458b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.