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  4. NDC Product Code: 50788-001 Honibe

NDC 50788-001 Honibe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50788-001?
  5. Honibe Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50788-001
Proprietary Name:
Honibe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Island Abbey Foods Ltd.
Labeler Code:
50788
Product Label ID:
d3645082-eb83-4a27-9dfe-79093dbe35ee
Start Marketing Date: [9]
05-30-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - HONEY YELLOW)
Shape:
ROUND (C48348)
Size(s):
16 MM
Imprint(s):
RAISED;FLOWER
Score:
1
Flavor(s):
LEMON (C73396 - LEMON OIL)

Code Structure Chart

Product Details

What is NDC 50788-001?

The NDC code 50788-001 is assigned by the FDA to the product Honibe which is product labeled by Island Abbey Foods Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50788-001-02 1 blister pack in 1 bag / 25 g in 1 blister pack (50788-001-01). 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 Honibe?

ADULTS AND CHILDREN 5 YEARS AND OVER:DISSOLVE 1 DROP SLOWLY IN MOUTH. REPEAT EVERY 2 HOURS AS NEEDED.CHILDREN UNDER 5 CONSULT  YOUR DOCTOR.

Which are Honibe UNII Codes?

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

Which are Honibe 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:

What is the NDC to RxNorm Crosswalk for Honibe?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

* 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".