Label: DR. C. TUNA SUN FACE AND BODY SPF 50- avobenzone, octinoxate, octocrylene, homosalate lotion
- NDC Code(s): 74690-015-01
- Packager: Farmasi US LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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- Drug Facts:
- Active Ingredient:
- Use:
- Warnings:
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Directions:
For Sunscreen Use
Apply generously 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. 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. Sun Protection Measures:
- Other Information:
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Inactive Ingredients:
Water/Aqua, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Glyceryl Stearate, Peg-100 Stearate, Glycerin, Ethylhexyl Palmitate, Ceteareth-20, Styrene/Acrylates Copolymer, Cyclopentasiloxane, Phenoxyethanol, Dimethicone, Adansonia Digitata Seed Oil, Calophyllum Inophyllum Seed Oil, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Tocopheryl Acetate, Ethylhexylglycerin.
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INGREDIENTS AND APPEARANCE
DR. C. TUNA SUN FACE AND BODY SPF 50
avobenzone, octinoxate, octocrylene, homosalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74690-015 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 25 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 65 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 90 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYL PALMITATE (UNII: 2865993309) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) STYRENE (UNII: 44LJ2U959V) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIMETHICONE (UNII: 92RU3N3Y1O) ADANSONIA DIGITATA SEED OIL (UNII: 77MKL7AR5I) TAMANU OIL (UNII: JT3LVK84A1) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) TROLAMINE (UNII: 9O3K93S3TK) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74690-015-01 1 in 1 BOX 07/25/2021 1 75 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 07/25/2021 Labeler - Farmasi US LLC (113303351)
