1. Home
  2. Labeler Index
  3. Tan-alize Kozmetik Ve Temizlik Urunleri Sanayi Ve Ticaret Anonim Sirketi
  4. NDC Product Code: 78317-000 Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body

NDC 78317-000 Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body

Avobenzone,Octinoxate,Octocrylene,Homosalate Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78317-000?
  4. Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
78317-000
Proprietary Name:
Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body
Non-Proprietary Name: [1]
Avobenzone, Octinoxate, Octocrylene, Homosalate
Substance Name: [2]
Avobenzone; Homosalate; Octinoxate; Octocrylene
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Tan-alize Kozmetik Ve Temizlik Urunleri Sanayi Ve Ticaret Anonim Sirketi
    Labeler Code:
    78317
    Product Label ID:
    a71ee8e0-2d27-7ae6-e053-2a95a90aecd4
    FDA Application Number: [6]
    M020
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    06-01-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 78317-000?

    The NDC code 78317-000 is assigned by the FDA to the product Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body which is a human over the counter drug product labeled by Tan-alize Kozmetik Ve Temizlik Urunleri Sanayi Ve Ticaret Anonim Sirketi. The generic name of Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body is avobenzone, octinoxate, octocrylene, homosalate. The product's dosage form is cream and is administered via topical form. The product is distributed in a single package with assigned NDC code 78317-000-01 1 tube in 1 box / 75 ml in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body?

    For suncreen use:-Applygenerously 15 minutes before sun exposure. - Reapply; - after 80 minutes of swimming or sweating - immediately  after towel drying  - at least  every 2 hours Sun Protection Measures; 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

    What are Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Dr. C Tuna Sunscreen 30 Spf Broad Spectrum Face And Body Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".