FLORMAR BLUR EFFECT BB SUNSCREEN BROAD SPECTRUM SPF 30 02 LIGHT MEDIUM- octinoxate, octocrylene, avobenzone cream

Flormar Blur Effect BB Sunscreen Broad Spectrum SPF 30 02 Light Medium by

Drug Labeling and Warnings

Flormar Blur Effect BB Sunscreen Broad Spectrum SPF 30 02 Light Medium by is a Otc medication manufactured, distributed, or labeled by Kosan Kozmetik Sanayi ve Ticaret A.S.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Octinoxate 5%

Octocrylene 2 %

Avobenzone 1 %

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

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wear alone or under foundation.
• Shake well before use.
• Apply liberally 15 minutes before sun exposure.
• Reapply at least every 2 hours.
• Use a water resistant sunscreen if swimming or sweating.
• 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 a Broad Spectrum SPF value of 30 or higher and other sun protection measures including:
• Limit time in the sun, especially from 10 a.m. - 2 p.m.
• Wear long-sleeved shirts, pants, hats and sunglasses.
• Children under 6 months of age: Ask a Doctor.

Other Information

• Protect the product in this container from excessive heat and direct sun.
• Keep the product cool.
• After use, close the tube properly with cap.

Inactive ingredients

water, cyclopentasiloxane, butylene glycol, polysilicone-11, cetyl PEG/PPG-10/1 dimethicone, dimethicone, PEG-10 dimethicone, trimethylsiloxysilicate, disteardimonium hectorite, synthetic fluorphlogopite, trimethylsiloxysilicate, SD alcohol 40-B, glycerin, dimethicone/vinyl dimethicone crosspolymer, phenoxyethanol, polyglyceryl-3 polydimethyl siloxyethyl dimethicone, polymethylsilsesquioxane, sodium chloride, stearic acid, silica, fragrance, ethylhexylglycerin, triethoxycaprylylsilane, magnesium stearate, aluminum hydroxide, algae extract, laureth-12, chlorophenesin, propylene glycol, camellia sinensis leaf extract, ilex paraguariensis leaf extract, paullinia cupana seed extract, sodium dehydroacetate. may contain: titanium dioxide, bismuth oxychloride, iron oxides.

Package Labeling:

INGREDIENTS AND APPEARANCE

FLORMAR BLUR EFFECT BB SUNSCREEN BROAD SPECTRUM SPF 30 02 LIGHT MEDIUM 
octinoxate, octocrylene, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61722-297
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	20 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
DIMETHICONE (UNII: 92RU3N3Y1O)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
STEARIC ACID (UNII: 4ELV7Z65AP)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
MAGNESIUM STEARATE (UNII: 70097M6I30)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-12 (UNII: OAH19558U1)
CHLORPHENESIN (UNII: I670DAL4SZ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
PAULLINIA CUPANA SEED (UNII: C21GE7524R)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61722-297-00	1 in 1 BOX	08/02/2016
1		35 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	08/02/2016

Labeler - Kosan Kozmetik Sanayi ve Ticaret A.S. (644090409)