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  4. NDC Product Code: 71801-542 Octisalate, Octocrylene, Octinoxate, Zinc Oxide, Titanium Dioxide, Ensulizole

NDC 71801-542 Octisalate, Octocrylene, Octinoxate, Zinc Oxide, Titanium Dioxide, Ensulizole

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71801-542?
  4. Octisalate, Octocrylene, Octinoxate, Zinc Oxide, Titanium Dioxide, Ensulizole 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:
71801-542
Proprietary Name:
Octisalate, Octocrylene, Octinoxate, Zinc Oxide, Titanium Dioxide, Ensulizole
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prokpil Sas
Labeler Code:
71801
Product Label ID:
6eafbc1c-44d8-5837-e053-2a91aa0ad979
Start Marketing Date: [9]
06-18-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 71801-542?

The NDC code 71801-542 is assigned by the FDA to the product Octisalate, Octocrylene, Octinoxate, Zinc Oxide, Titanium Dioxide, Ensulizole 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 71801-542-01 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 Octisalate, Octocrylene, Octinoxate, Zinc Oxide, Titanium Dioxide, Ensulizole?

Apply liberally 15 minutes before sun exposureUse water resistant sun protector if swimming or sweating. Reapply at least every two hours. Children under six months: ask a doctor 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.

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

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

Which are Octisalate, Octocrylene, Octinoxate, Zinc Oxide, Titanium Dioxide, Ensulizole 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".