Label: TRILIPIDERM PROTECTIVE DAY- homosalate, ethylhexyl methoxycinnamate,butyl methoxydibenzoylmethane, octocrylene cream
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NDC Code(s):
60892-602-15,
60892-602-16,
60892-602-32,
60892-602-33, view more60892-602-77
- Packager: TriLipid Research Institute, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- Stop use and ask a doctor
- When using this product
- Keep out of reach of children.
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Directions:
- Apply liberally 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating
- Reapply 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 10:00 AM – 2:00 PM
- Wear long sleeved shirts, pants, hats, and sunglasses
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Inactive Ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aqua (Deionized Water), I-Arginine, Ascorbic Acid (Vitamin C), Benzoic Acid, Cetearyl Alcohol, Chamomilla Matricaria (Chamomile) Extract, Cholecalciferol (Vitamin D3), Crambe Abyssinica (Abyssinian) 0il, Ethylhexylglycerin, Gluconolactone, Glycerin, Glyceryl Stearate, Limnanthes Alba (Meadowfoam) Seed Oil, Olea Europaea (Olive) Fruit Unsaponifiables, Phenoxyethanol, Polysorbate-20, Polysorbate-60, Retinyl Palmitate (Vitamin A), Sodium Hyaluronate, Sodium Ascorbyl Phosphate (Vitamin C), Sodium Hydroxide, Squalane, Tocopheryl Acetate (Vitamin E)
- Other Information
- TriLipiderm Protective Day Creme
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INGREDIENTS AND APPEARANCE
TRILIPIDERM PROTECTIVE DAY
homosalate, ethylhexyl methoxycinnamate,butyl methoxydibenzoylmethane, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60892-602 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2.7 g in 100 mL Inactive Ingredients Ingredient Name Strength CRAMBE HISPANICA SUBSP. ABYSSINICA WHOLE (UNII: 3885PD1IZ8) GLUCONOLACTONE (UNII: WQ29KQ9POT) PHENOXYETHANOL (UNII: HIE492ZZ3T) SQUALANE (UNII: GW89575KF9) SODIUM HYDROXIDE (UNII: 55X04QC32I) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) ASCORBIC ACID (UNII: PQ6CK8PD0R) CHOLECALCIFEROL (UNII: 1C6V77QF41) MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT) POLYSORBATE 60 (UNII: CAL22UVI4M) BENZOIC ACID (UNII: 8SKN0B0MIM) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYSORBATE 20 (UNII: 7T1F30V5YH) CHAMOMILE (UNII: FGL3685T2X) VITAMIN A (UNII: 81G40H8B0T) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) WATER (UNII: 059QF0KO0R) ARGININE (UNII: 94ZLA3W45F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60892-602-33 1 in 1 BOX 12/12/2018 1 NDC:60892-602-32 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:60892-602-77 4 mL in 1 PACKET; Type 0: Not a Combination Product 12/12/2018 3 NDC:60892-602-16 1 in 1 BOX 12/23/2018 3 NDC:60892-602-15 15 mL in 1 BOTTLE; 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 12/12/2018 Labeler - TriLipid Research Institute, LLC (013903326)