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  4. NDC Product Code: 70797-230 Nuby Teething Gel

NDC 70797-230 Nuby Teething Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70797-230?
  5. Nuby Teething Gel 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:
70797-230
Proprietary Name:
Nuby Teething Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Talbot�s Pharmaceuticals Family Products, Llc.
Labeler Code:
70797
Product Label ID:
365e0605-b635-226e-e054-00144ff88e88
Start Marketing Date: [9]
12-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
TUTTI FRUTTI (C73420)

Product Packages

NDC Code 70797-230-24

Package Description: 24 CARTON in 1 CARTON / 4 BLISTER PACK in 1 CARTON / 1 TUBE in 1 BLISTER PACK / 15 g in 1 TUBE (70797-230-15)

Product Details

What is NDC 70797-230?

The NDC code 70797-230 is assigned by the FDA to the product Nuby Teething Gel which is product labeled by Talbot�s Pharmaceuticals Family Products, Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70797-230-24 24 carton in 1 carton / 4 blister pack in 1 carton / 1 tube in 1 blister pack / 15 g in 1 tube (70797-230-15). 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 Nuby Teething Gel?

Wash hands before use.Cut open tip of tube on score mark.Use your finger tip or cotton applicator to gently apply a small pea-size amount of Nuby Teething Gel to the affected area up to 4 times daily or as directed by a physician or healthcare provider.For infants under 4 months of age, ask a dentist or doctor before use.

Which are Nuby Teething Gel UNII Codes?

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

Which are Nuby Teething Gel 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 Nuby Teething Gel?

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 indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".