LC FOUNDATION SPF 15 cream

LC FOUNDATION SPF 15 by

Drug Labeling and Warnings

LC FOUNDATION SPF 15 by is a Otc medication manufactured, distributed, or labeled by MANA Products INC., MANA PRODUCTS, INC., MANA PRODUCTS, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Titanium Dioxide 5.00%

Zinc Oxide 5.00%

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.

DIRECTIONS

For sunscreen use:

Shake well.
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 risk of skin cancer and early 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 10:00 a.m. - 2:00 p.m.
wear long sleeved shirts, pants, hats and sunglasses.
Children under 6 months of age: ask a doctor.

INACTIVE INGREDIENTS

Water (Aqua/Eau), Ethylhexyl Palmitate, Dimethicone, PEG-30 Dipolyhydroxystearate, Butylene Glycol, Neopentyl Glycol Diethylhexanoate, Triethylhexanoin, Caprylic/Capric Triglyceride, Octyldodecyl Neopentanoate, Glycerin, Silica, Tremella Fuciformis Sporocarp Extract, Butyrospermum Parkii (Shea) Butter, Tocopherol, Tocopheryl Acetate, Sodium Hyaluronate, Dimethicone Crosspolymer-3, Simethicone, Betaine, Octyldodecanol, Phytantriol, Disteardimonium Hectorite, Tribehenin, Lysine, Magnesium Chloride, Potassium Chloride, Zinc Chloride, Sodium Chloride, Triethoxycaprylylsilane, Sodium Citrate, Citric Acid, Hexylene Glycol, Potassium Sorbate, Capr ylyl Glycol, Phenoxyethanol. May Contain (+/-): Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, 77492, 77499)

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

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

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LC FOUNDATION SPF 15 
lc foundation spf 15 cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59735-401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	5 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
LYSINE (UNII: K3Z4F929H6)
ZINC CHLORIDE (UNII: 86Q357L16B)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
DIMETHICONE (UNII: 92RU3N3Y1O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)
TOCOPHEROL (UNII: R0ZB2556P8)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
BETAINE (UNII: 3SCV180C9W)
OCTYLDODECANOL (UNII: 461N1O614Y)
PHYTANTRIOL (UNII: 8LVI07A72W)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
WATER (UNII: 059QF0KO0R)
PEG-30 DIPOLYHYDROXYSTEARATE (5000 MW) (UNII: 9713Q0S7FO)
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
GLYCERIN (UNII: PDC6A3C0OX)
SHEA BUTTER (UNII: K49155WL9Y)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)

Product Characteristics
Color	white (SHADE 3.0)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59735-401-01	30 g in 1 TUBE; Type 0: Not a Combination Product	08/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	08/25/2020

Labeler - MANA Products INC. (078870292)

Establishment
Name	Address	ID/FEI	Business Operations
MANA PRODUCTS, INC		032870270	manufacture(59735-401)

Establishment
Name	Address	ID/FEI	Business Operations
MANA PRODUCTS, INC.		078870292	manufacture(59735-401)