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  4. NDC Product Code: 80732-304 Oleander 4x

NDC 80732-304 Oleander 4x

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 80732-304?
  5. Oleander 4x Uses
  6. Active Ingredients UNII Codes
  7. 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:
80732-304
Proprietary Name:
Oleander 4x
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avila Herbals
Labeler Code:
80732
Product Label ID:
b001ba11-f634-29a8-e053-2995a90ab7c6
Start Marketing Date: [9]
10-19-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
ORANGE (C73406)

Code Structure Chart

Product Details

What is NDC 80732-304?

The NDC code 80732-304 is assigned by the FDA to the product Oleander 4x which is product labeled by Avila Herbals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80732-304-11 1 u 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 Oleander 4x?

Take 1ml every 6 hours; not more than 4 ml in a 24 hour period

Which are Oleander 4x UNII Codes?

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

Which are Oleander 4x 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".