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  4. NDC Product Code: 65923-633 Family Care Cough And Cold

NDC 65923-633 Family Care Cough And Cold

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65923-633?
  4. Family Care Cough And Cold 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:
65923-633
Proprietary Name:
Family Care Cough And Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
United Exchange Corp.
Labeler Code:
65923
Product Label ID:
3bb3a81d-d39a-4f79-84f1-ab0c075d7d34
Start Marketing Date: [9]
07-29-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 65923-633-04

Package Description: 118 mL in 1 BOTTLE

Product Details

What is NDC 65923-633?

The NDC code 65923-633 is assigned by the FDA to the product Family Care Cough And Cold which is product labeled by United Exchange Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65923-633-04 118 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 Family Care Cough And Cold?

Directionsdo not take more than 6 doses in any 24-hour periodmeasure only with dosing cup provided. Keep dosing cup with productmL = milliliterthis adult product is not intended for use in children under 12 years of age age dose adults and children 12 years and over 10 mL every 4 hours children under 12 years do not use

Which are Family Care Cough And Cold UNII Codes?

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

Which are Family Care Cough And Cold 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".