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  4. NDC Product Code: 71801-541 Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide

NDC 71801-541 Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71801-541?
  4. Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71801-541
Proprietary Name:
Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prokpil Sas
Labeler Code:
71801
Product Label ID:
5c4230af-280e-2b73-e053-2991aa0aa4a9
Start Marketing Date: [9]
09-01-2017
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71801-541-01

Package Description: 30 g in 1 BOX

Product Details

What is NDC 71801-541?

The NDC code 71801-541 is assigned by the FDA to the product Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide which is product labeled by Prokpil Sas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71801-541-01 30 g in 1 box . 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 Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide?

Apply generously and evenly 15 minutes before sun exposureReapply at least every two hours Use water resistant sun protector if swimming or sweating. Sun protection measures: Overexposure to the sun is dangerous. Increases the risk of causing skin cancer and premature aging. To reduce the risk, regularly use sunscreen with broad spectrum SPF 15 or higher, combined with other sun protection measures. Limit exposure time especially between 10 am - 2 pm. Wear long sleeves, hat and glasses. Children under 6 months of age ask a doctor.

Which are Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide UNII Codes?

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

Which are Octinoxate, Octisalate, Avobenzone, Octocrylene, Ensulizole, Titanium Dioxide 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:

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Product Footnotes

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

[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".