FLORIDA GLOW SPF 30- avobenzone,octocrylene,octisalate,homosalate spray

Florida Glow SPF 30 by

Drug Labeling and Warnings

Florida Glow SPF 30 by is a Otc medication manufactured, distributed, or labeled by Southeast Holdings Corp., Southeast Holdings Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients                    

Homosalate 7%
Octisalate 5%                          
Octocrylene 5%
Avobenzone 3%

Purpose

Sunscreen

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.

Warnings

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 he$ or contact a Po1son Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Directions

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

SD Alcohol 40-8, 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

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

INGREDIENTS AND APPEARANCE

FLORIDA GLOW SPF 30 
avobenzone,octocrylene,octisalate,homosalate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83862-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
COCONUT OIL (UNII: Q9L0O73W7L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DIBUTYL MALEATE (UNII: 4X371TMK9K)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83862-002-01	162 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/19/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/19/2021

Labeler - Southeast Holdings Corp. (122400191)

Establishment
Name	Address	ID/FEI	Business Operations
Southeast Holdings Corp		080504027	label(83862-002) , pack(83862-002) , manufacture(83862-002)