Label: DR. C. TUNA SUNSCREEN 50 SPF UVA UVB PROTECTION FACE AND BODY SUN- avobenzone, octinoxate, octocrylene, homosalate lotion
- NDC Code(s): 74690-006-01
- Packager: Farmasi US LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 9, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- PURPOSE
- Uses
- Warnings
-
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: Ask a doctor. Sun Protection Measures:
- Other information
-
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.
- Questions or Comments?
-
SPL UNCLASSIFIED SECTION
Manufactured by: Tan-Alize Kozmetik ve Temizlik Ürünleri San. ve. Tic. A.S. Ömerli Mah. Uran Cad. No: 32 / 34797 Cekmeköy / ISTANBUL
Made in TURKEY
EU REsponsible Person: Farmasi Central Europe S.R.O. Stará Vajnorská Republika. Distributed By: FARMASI US LLC 2315 NW 107 TH AVE, STE 1B 12, DORAL , FL 33172.
- Package Labeling
-
INGREDIENTS AND APPEARANCE
DR. C. TUNA SUNSCREEN 50 SPF UVA UVB PROTECTION FACE AND BODY SUN
avobenzone, octinoxate, octocrylene, homosalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74690-006 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) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIMETHICONE (UNII: 92RU3N3Y1O) ADANSONIA DIGITATA SEED OIL (UNII: 77MKL7AR5I) TAMANU OIL (UNII: JT3LVK84A1) TROLAMINE (UNII: 9O3K93S3TK) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74690-006-01 75 mL in 1 TUBE; Type 0: Not a Combination Product 01/08/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/08/2020 Labeler - Farmasi US LLC (113303351) Establishment Name Address ID/FEI Business Operations TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI 365979587 manufacture(74690-006)
