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  4. NDC Product Code: 58331-050 Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire

NDC 58331-050 Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire

Homosalate,Octisalate,Octocrylene,Oxybenzone,And Avobenzone Lotion Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58331-050?
  4. Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
58331-050
Proprietary Name:
Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire
Non-Proprietary Name: [1]
Homosalate, Octisalate, Octocrylene, Oxybenzone, And Avobenzone
Substance Name: [2]
Avobenzone; Homosalate; Octisalate; Octocrylene; Oxybenzone
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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]
    Degil Safety Products (1989) Inc.
    Labeler Code:
    58331
    Product Label ID:
    59999fef-259d-4077-8ebb-e884541973a0
    FDA Application Number: [6]
    part352
    Marketing Category: [8]
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date: [9]
    02-18-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 58331-050-01

    Package Description: 120 mL in 1 BOTTLE, PLASTIC

    NDC Code 58331-050-02

    Package Description: 10 mL in 1 PACKET

    NDC Code 58331-050-03

    Package Description: 750 mL in 1 BOTTLE, PLASTIC

    Product Details

    What is NDC 58331-050?

    The NDC code 58331-050 is assigned by the FDA to the product Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire which is a human over the counter drug product labeled by Degil Safety Products (1989) Inc.. The generic name of Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire is homosalate, octisalate, octocrylene, oxybenzone, and avobenzone. The product's dosage form is lotion and is administered via topical form. The product is distributed in 3 packages with assigned NDC codes 58331-050-01 120 ml in 1 bottle, plastic , 58331-050-02 10 ml in 1 packet , 58331-050-03 750 ml in 1 bottle, plastic . 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 Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire?

    Apply liberally and evenly to dry skin 15 minutes before exposure to the sun. Reapply every 2 hours to insure adequate UV protection or 80 minutes after swimming, perspiring heavily, or immediately after washing and towel drying.For children under 6 months of age: Ask a doctor

    What are Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire 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 Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire UNII Codes?

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

    Which are Croc Bloc Broad Spectrum Spf 50 Fps Ecran Solaire 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".