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NDC 69226-010 Reman Homme Sun Protection

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69226-010?
  4. Reman Homme Sun Protection 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:
69226-010
Proprietary Name:
Reman Homme Sun Protection
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pf Nature
Labeler Code:
69226
Product Label ID:
7bea7d8a-b868-4163-ac04-459159e71e9e
Start Marketing Date: [9]
09-30-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69226-010?

The NDC code 69226-010 is assigned by the FDA to the product Reman Homme Sun Protection which is product labeled by Pf Nature. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69226-010-01 22 g in 1 carton . 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 Reman Homme Sun Protection?

Indication and usage:Please close the cap after use. Once it is unpacked, please use them up immediately as it dries up quickly.Please do not keep this product in places with very high or low temperatures.And please keep it out of direct sunlight.

Which are Reman Homme Sun Protection UNII Codes?

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

Which are Reman Homme Sun Protection 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

[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".