LANEIGE SKIN VEIL BASE EX NO.40 LIGHT PURPLE- octinoxate lotion LANEIGE SKIN VEIL BASE EX NO.60 LIGHT GREEN- octinoxate lotion

LANEIGE SKIN VEIL BASE EX No.60 Light Green by

Drug Labeling and Warnings

LANEIGE SKIN VEIL BASE EX No.60 Light Green by is a Otc medication manufactured, distributed, or labeled by AMOREPACIFIC CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENTS

ETHYLHEXYL METHOXYCINNAMATE 6.5%

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 value of 15 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

INACTIVE INGREDIENTS

WATER, CYCLOPENTASILOXANE, DIMETHICONE, CYCLOHEXASILOXANE, BUTYLENE GLYCOL, GLYCERIN, C 12-15 ALKYL BENZOATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, TITANIUM DIOXIDE (CI 77891), LAURYL PEG- 9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, DISTEARDIMONIUM HECTORITE, PEG/PPG- 19/19 DIMETHICONE, ULTRAMARINES (CI 77007), POLYMETHYL METHACRYLATE, SODIUM CHLORIDE, HYDROGENATED POLYDECENE, BORON NITRIDE, METHYL METHACRYLATE CROSSPOLYMER, PHENOXYETHANOL, FRAGRANCE, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, ALUMINUM HYDROXIDE, TRIETHOXYCAPRYLYLSILANE, DISODIUM EDTA, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, TOCOPHEROL

OTHER INFORMATION

• Protect the product in this container from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - No. 40 Light Purple

LANEIGE

Skin Veil Base EX
broad spectrum
SPF 22 sunscreen

30 mL / 1.0 FL. OZ. e

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton - No. 60 Light Green

LANEIGE

Skin Veil Base EX
broad spectrum
SPF 22 sunscreen

30 mL / 1.0 FL. OZ. e

INGREDIENTS AND APPEARANCE

LANEIGE SKIN VEIL BASE EX NO.40 LIGHT PURPLE 
octinoxate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43419-712
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.95 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
ULTRAMARINE BLUE (UNII: I39WR998BI)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
BORON NITRIDE (UNII: 2U4T60A6YD)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43419-712-02	1 in 1 CARTON	04/21/2014	06/08/2020
1		30 mL in 1 BOTTLE, PUMP; 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	04/21/2014	06/08/2020

LANEIGE SKIN VEIL BASE EX NO.60 LIGHT GREEN 
octinoxate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43419-713
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.95 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BORON NITRIDE (UNII: 2U4T60A6YD)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
CHROMIC OXIDE (UNII: X5Z09SU859)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ULTRAMARINE BLUE (UNII: I39WR998BI)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43419-713-02	1 in 1 CARTON	04/21/2014	06/09/2020
1		30 mL in 1 BOTTLE, PUMP; 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	04/21/2014	06/09/2020

Labeler - AMOREPACIFIC CORPORATION (631035289)

Establishment
Name	Address	ID/FEI	Business Operations
AMOREPACIFIC CORPORATION		694894112	manufacture(43419-712, 43419-713)