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  4. NDC Product Code: 70314-201 Facial With Placenta Protein Spf-15

NDC 70314-201 Facial With Placenta Protein Spf-15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70314-201?
  4. Facial With Placenta Protein Spf-15 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:
70314-201
Proprietary Name:
Facial With Placenta Protein Spf-15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bill Beauty And Health Products Ltd
Labeler Code:
70314
Product Label ID:
240d21b9-6dcf-4990-b8a2-7791246d563c
Start Marketing Date: [9]
12-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70314-201?

The NDC code 70314-201 is assigned by the FDA to the product Facial With Placenta Protein Spf-15 which is product labeled by Bill Beauty And Health Products Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70314-201-11 90 ml in 1 bottle , 70314-201-21 180 ml in 1 bottle . 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 Facial With Placenta Protein Spf-15?

Apply generously 15 minutes before sun exposure. Reapply at least every 2 hours. For use on children less than 6 months of age, consult a health care professional. Use a water resistant sunscreen if swimming or sweating.

Which are Facial With Placenta Protein Spf-15 UNII Codes?

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

Which are Facial With Placenta Protein Spf-15 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".