Label: LAUREN CONRAD - THE LIQUID FOUNDATION SPF 15- titanium dioxide, zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 80261-101-01 - Packager: Lauren Conrad Beauty Co.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 31, 2020
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- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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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.
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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)
- OTHER INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LAUREN CONRAD - THE LIQUID FOUNDATION SPF 15
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80261-101 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 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Ethylhexyl Palmitate (UNII: 2865993309) Dimethicone (UNII: 92RU3N3Y1O) PEG-30 Dipolyhydroxystearate (UNII: 9713Q0S7FO) Butylene Glycol (UNII: 3XUS85K0RA) Neopentyl Glycol Diethylhexanoate (UNII: U68ZV6W62C) Triethylhexanoin (UNII: 7K3W1BIU6K) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Octyldodecyl Neopentanoate (UNII: X8725R883T) Glycerin (UNII: PDC6A3C0OX) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G) SHEA BUTTER (UNII: K49155WL9Y) TOCOPHEROL (UNII: R0ZB2556P8) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYALURONATE SODIUM (UNII: YSE9PPT4TH) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) BETAINE (UNII: 3SCV180C9W) OCTYLDODECANOL (UNII: 461N1O614Y) PHYTANTRIOL (UNII: 8LVI07A72W) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIBEHENIN (UNII: 8OC9U7TQZ0) LYSINE (UNII: K3Z4F929H6) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) ZINC CHLORIDE (UNII: 86Q357L16B) SODIUM CHLORIDE (UNII: 451W47IQ8X) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SODIUM CITRATE (UNII: 1Q73Q2JULR) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) HEXYLENE GLYCOL (UNII: KEH0A3F75J) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80261-101-01 30 mL 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 not final part352 08/25/2020 Labeler - Lauren Conrad Beauty Co. (123316147) Establishment Name Address ID/FEI Business Operations MANA PRODUCTS, INC. 078870292 manufacture(80261-101)