Home › NDC Lookup › Ingredients › Avobenzone, Octinoxate, Octocrylene, Hom... › 78317-0000-01
DR. C Tuna Sunscreen 30 SPF Broad Spectrum Face and body AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE 15 mg/mL; 50 mg/mL; 50 mg/mL; 70 mg/mL Cream — NDC 78317-0000-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

DR. C Tuna Sunscreen 30 SPF Broad Spectrum Face and body AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE 15 mg/mL; 50 mg/mL; 50 mg/mL; 70 mg/mL Cream — NDC 78317-000-01 (Billing 78317-0000-01)

by TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI · 1 TUBE in 1 BOX / 75 mL in 1 TUBE

This is a package of DR. C Tuna Sunscreen 30 SPF Broad Spectrum Face and body AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE 15 mg/mL; 50 mg/mL; 50 mg/mL; 70 mg/mL Cream from TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI, marketed since Jun 2020 and currently FDA-listed. It is this product's only package size.

NDC 78317-0000-01
🏷️ FDA NDC (as labeled) 78317-000-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 78317-000-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
78317 labeler · 000 product · 01 package
Package marketed since
Jun 1, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7831700001 4
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 78317-000-01
Product NDC 78317-000
11-digit billing NDC 78317000001
UNII G63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM, V06SV4M95S
Application # M020
SPL Set ID a71ee8e0-2d27-7ae6-e053-2a95a90aecd4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-06-01
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTINOXATE; OCTOCRYLENE; HOMOSALATE
Why two NDCs? The FDA registers this code as 78317-000-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 78317-0000-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

DR. C Tuna Sunscreen 30 SPF Broad Spectrum is a topical cream containing four UV-filtering ingredients: avobenzone, homosalate, octinoxate, and octocrylene. These active ingredients are commonly used together in sunscreen products to absorb and scatter ultraviolet light from the sun. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for sunscreen products rather than as an individually reviewed application. The product is intended for application to the face and body.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
78317-0000-01 You're viewing this Main listing 1 TUBE in 1 BOX / 75 mL in 1 TUBE 2020-06-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
DR. C Tuna Sunscreen 30 SPF Broad Spectrum Face and body 15 mg/mL; 50 mg/mL; 50 mg/mL; 70 mg/mLthis 78317-0000-01 TAN-ALIZE 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2020
On the market since
Jun 2020
📍
2026
Currently FDA-listed
6 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII J94PBK7X8S
    A synthetic polymer derived from acrylic acid monomers. In medicines, it's used as a binder to hold tablet ingredients together and sometimes as a coating agent to control where and how the drug releases in the body.
  • UNII 77MKL7AR5I
    A natural oil extracted from baobab tree seeds. It's used as an emollient and skin-conditioning agent to help soften the product texture and improve how the medicine feels on application.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII 01YAE03M7J
    Beta carotene is a naturally occurring orange pigment found in plants. In medicines, it serves as a colorant to make tablets or capsules appear orange or yellow.
  • UNII L56Z1JK48B
    A vegetable-derived ingredient used primarily as a natural colorant and flavoring agent in medicines. It provides orange-yellow color and mild taste to tablets, capsules, or liquids.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII 2865993309
    Ethylhexyl palmitate is an oily chemical made from palm oil and alcohol. It acts as an emollient and skin-conditioning agent in topical medicines, helping the product spread smoothly and keeping skin soft.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII YRC528SWUY
    A waxy emulsifier made from plant-derived fatty alcohols. It helps blend oil and water-based ingredients together and improves how the medicine spreads and absorbs.
  • UNII 241ATL177A
    Soybean oil is a natural plant oil derived from soybean seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients and improve how the body absorbs them.
  • UNII 44LJ2U959V
    Styrene is a liquid synthetic chemical used as a solvent and plasticizer in some pharmaceutical coatings and film formulations. It helps dissolve active ingredients and creates flexible protective layers around tablets or capsules.
  • UNII JT3LVK84A1
    A plant-based oil extracted from tamanu tree nuts, used as an emollient and skin-conditioning agent in topical formulations. It helps soften and moisturize the product's texture.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

22 inactive ingredients listed in the exact product block matched to this NDC.

The official label also stateswater/Aqua, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Glyceryl Stearate, Peg-100 Stearate, Glycerin, Ethylhexyl Palmitate,Ceteareth-20, Styrene/Acrylates Copolymer, Cyclopentasiloxane, Phenoxyethonol, Dimethicone, Adansonia digitata Seed Oil, Calophyllum inophyllum Seed Oil, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Glycine Soja Oil, Daucus Carota Sativa Root Extract, Beta-Carotene, Tocopherol, Triethanolamine, Tocopheryl Acetate, ethlhexylglycerin.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerTAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code78317
First marketedJun 2020
Product typeHuman Otc Drug

More NDCs from TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI V... labeler code 78317

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

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.

⏱️ Dosage and Administration 107 words ▾

Directions For suncreen use: -Apply generously 15 minutes before sun exposure. - Reapply; - after 80 minutes of swimming or sweating - immediately after towel drying - at least every 2 hours ; Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk, regular use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including; - limit in the sun, especially from 10 a.m -2 p.m. - wear long - sleeved shirts, pants, hats and sun glasses - children under 6 months of age: Ask a doctor Sun Protection Measures

⚠️ Warnings 53 words ▾

Warnings For external use only. -Do not use on damaged or broken skin. -When using this product keep out of eyes. Rinse with water to remove. -Stop use and ask doctor if rash occurs. -Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Centre right away

🧪 Active Ingredient 14 words ▾

Active Ingredients Butyl Methoxydibenzoylmethane 1.5% ethylhexyl Methoxycinnamate 5%, Octocrylene 5%, Homosalate 7% purpose Sunscreen

🧪 Inactive Ingredients 47 words ▾

Inactive Ingredients water/Aqua, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Glyceryl Stearate, Peg-100 Stearate, Glycerin, Ethylhexyl Palmitate,Ceteareth-20, Styrene/Acrylates Copolymer, Cyclopentasiloxane, Phenoxyethonol, Dimethicone, Adansonia digitata Seed Oil, Calophyllum inophyllum Seed Oil, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Glycine Soja Oil, Daucus Carota Sativa Root Extract, Beta-Carotene, Tocopherol, Triethanolamine, Tocopheryl Acetate, ethlhexylglycerin.

🎯 Purpose 2 words ▾

purpose Sunscreen

📄 Do Not Use 8 words ▾

-Do not use on damaged or broken skin.

📄 When Using This Product 13 words ▾

-When using this product keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 8 words ▾

-Stop use and ask doctor if rash occurs.

📄 Keep Out of Reach of Children 19 words ▾

-Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Centre right away

📄 Questions or Comments 18 words ▾

Questions or comments? [email protected] +1 (833) 432 76 27 Monday - Friday (9 a.m - 6 p.m. EST)

📄 Package Label / Principal Display Panel 3 words ▾

Package Labeling: Bottle

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
TAN-ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 78283-0007-01 · BERIOSKA 78317-0027-01 · Tan →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.