Label: PEPTIDE LIP SHINE SPF30 SUNSCREEN- zinc oxide liquid
- NDC Code(s): 68078-080-01
- Packager: Colorescience, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
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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
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DOSAGE & ADMINISTRATION
Apply liberally 15 minutes before sun exposure. Works best on moisturized skin. Reapply:
- After 40 minutes of swimming or sweating.
- Immediately after towel drying.
- At least every 2 hours.
Children under 6 months: ask a doctor.
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.
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Inactive ingredients
Phenyl Trimethicone, Bis-Vinyl Dimethicone/ Dimethicone Copolymer, Neopentyl Glycol Diheptanoate, Disteardimonium Hectorite, Mica, Ethylhexyl Palmitate, Tocopheryl Acetate, Triethyl Citrate, Glyceryl Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Polyhydroxystearic Acid, Tribehenin, Sodium Hyaluronate, Palmitoyl Tripeptide-1, Sorbitan Isostearate, Tin Oxide, Flavor/Aroma, Limonene, Iron Oxides (CI 77491, CI 77492, CI 77499), Titanium Dioxide (CI 77891), Carmine (CI 75470). Contains Carmine as a color additive.
- Other Information
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 4 mL Tube Carton
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INGREDIENTS AND APPEARANCE
PEPTIDE LIP SHINE SPF30 SUNSCREEN
zinc oxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68078-080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 78 mg in 1 mL Inactive Ingredients Ingredient Name Strength Phenyl Trimethicone (UNII: DR0K5NOJ4R) Neopentyl Glycol Diheptanoate (UNII: 5LKW3C543X) Disteardimonium Hectorite (UNII: X687XDK09L) MICA (UNII: V8A1AW0880) Ethylhexyl Palmitate (UNII: 2865993309) Triethyl Citrate (UNII: 8Z96QXD6UM) Glyceryl Isostearate (UNII: HYE7O27HAO) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) Tribehenin (UNII: 8OC9U7TQZ0) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Palmitoyl Tripeptide-1 (UNII: RV743D216M) Sorbitan Isostearate (UNII: 01S2G2C1E4) LIMONENE, (+)- (UNII: GFD7C86Q1W) STANNIC OXIDE (UNII: KM7N50LOS6) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) CARMINIC ACID (UNII: CID8Z8N95N) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68078-080-01 1 in 1 CARTON 10/01/2024 1 4 mL in 1 TUBE, WITH APPLICATOR; 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 10/01/2024 Labeler - Colorescience, Inc. (128731929)