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  4. NDC Product Code: 59779-642 Infants Teething Liquid

NDC 59779-642 Infants Teething Liquid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59779-642?
  5. Infants Teething Liquid 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:
59779-642
Proprietary Name:
Infants Teething Liquid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy
Labeler Code:
59779
Product Label ID:
518069c3-6c91-43fa-9e7b-ba7d244cfb8b
Start Marketing Date: [9]
02-25-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
ORANGE (C73406)

Code Structure Chart

Product Details

What is NDC 59779-642?

The NDC code 59779-642 is assigned by the FDA to the product Infants Teething Liquid which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-642-02 1 bottle in 1 carton / 25 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 Infants Teething Liquid?

Do not use more than directed.Do not take with food.Take 0.75 mL orally at the onset of pain.Repeat every 15 minutes up to 4 times daily then reduce with improvement until pain subsides, or as directed by a healthcare professional.Age: Infants and children 0 to 9 years of ageDose: 0.75 mL

Which are Infants Teething Liquid UNII Codes?

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

Which are Infants Teething Liquid 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".