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NDC 78362-803 Viiva Bioderma Actives Hgh Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78362-803?
  4. Viiva Bioderma Actives Hgh Cream 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:
78362-803
Proprietary Name:
Viiva Bioderma Actives Hgh Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Viiva Llc
Labeler Code:
78362
Product Label ID:
5d5dc075-8578-4246-affa-79d286b2e44c
Start Marketing Date: [9]
04-15-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 78362-803?

The NDC code 78362-803 is assigned by the FDA to the product Viiva Bioderma Actives Hgh Cream which is product labeled by Viiva Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78362-803-01 100 g in 1 bottle, pump . 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 Viiva Bioderma Actives Hgh Cream?

Apply 2 full pumps in the morning and 2 full pumps in the evening.For intensive use, apply 2 full pumps three times a day.Cream should always be applied to thin areas of the skin where veins are visible.You may apply the cream to your face, wrists, underarms, forearms or behind the knees. Application sites should be rotated. If pregnant or breastfeeding, ask a health care professional before use.FOR EXTERNAL USE ONLY

Which are Viiva Bioderma Actives Hgh Cream UNII Codes?

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

Which are Viiva Bioderma Actives Hgh Cream 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".