SUN LOGIC LAIT SOLAIRE CORPS SPF 20- avobenzone, homosalate, octocrylene lotion

Sun Logic Lait Solaire Corps SPF 20 by

Drug Labeling and Warnings

Sun Logic Lait Solaire Corps SPF 20 by is a Otc medication manufactured, distributed, or labeled by Guinot. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Avobenzone 2.90%

Homosalate 12.00%

Octocrylene 2.70%

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

Directions

• 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 of 15 or higher and other sun protection measures including:

- Limit time in the sun, especially from 10 a.m. to 2 p.m.

- Wear long-sleeve shirts, pants, hats, and sunglasses

• Children under 6 months: Ask a doctor.

Other information

• Protect this product from excessive heat and direct sun
• Store below 30°C/86°F

Inactive ingredients

Water/Eau (Aqua), Dibutyl Adipate, Ethylhexyl Palmitate, Caprylyl Methicone, Diethylhexyl 2,6-Naphthalate, Polyethylene, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Squalane, Caprylyl Glycol, Propylene Glycol, Sodium Stearoyl Glutamate, Tocopheryl Acetate, Fragrance (Parfum), Glycerin, Polysorbate 60, Butylene Glycol, Betaine, Hydrolyzed Enteromorpha Compressa, Limonene, Sorbitan Isostearate, Citric Acid, Pectin, Sucrose, Alpha-Isomethyl Ionone, Glyceryl Acrylate/Acrylic Acid Copolymer, Ethylhexylglycerin, Oleoyl Tyrosine, Capryloyl Glycine, Sodium Hyaluronate, Oleic Acid, Copper Gluconate. 01

Package Labeling:

INGREDIENTS AND APPEARANCE

SUN LOGIC LAIT SOLAIRE CORPS SPF 20 
avobenzone, homosalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54181-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	29 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	120 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	27 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIBUTYL ADIPATE (UNII: F4K100DXP3)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
SQUALANE (UNII: GW89575KF9)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 60 (UNII: CAL22UVI4M)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
BETAINE (UNII: 3SCV180C9W)
HYDROLYZED ULVA COMPRESSA PROTEIN (ACID; 300-5000 MW) (UNII: Q04O53779D)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PECTIN (UNII: 89NA02M4RX)
SUCROSE (UNII: C151H8M554)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
OLEOYL TYROSINE (UNII: 131P1BQX1U)
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
OLEIC ACID (UNII: 2UMI9U37CP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54181-010-00	1 in 1 BOX	12/23/2017
1		150 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 Drug	M020	12/23/2017

Labeler - Guinot (763667185)

Establishment
Name	Address	ID/FEI	Business Operations
Guinot		763667185	manufacture(54181-010)