70797-240 NDC - NUBY SOOTHING GEL ()

Drug Information

  • Product NDC: 70797-240
  • Proprietary Name: Nuby Soothing Gel
  • Non Proprietary Name:
  • Active Ingredient(s): 30 [hp_X]/15g ARNICA MONTANA ROOT; 12 [hp_X]/15g MATRICARIA RECUTITA; 12 [hp_X]/15g TRIBASIC CALCIUM PHOSPHATE
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Blood Coagulation Factor [EPC]; Calcium [CS]; Cations; Divalent [CS]; Increased Coagulation Factor Activity [PE]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]

Labeler Information

Field Name Field Value
Labeler Name: Talbot's Pharmaceuticals Family Products, LLC.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/25/2018

Package Information

No. Package Code Package Description Billing Unit
170797-240-011 TUBE in 1 BLISTER PACK (70797-240-01) / 15 g in 1 TUBE (70797-240-15)
270797-240-021 TUBE in 1 BLISTER PACK (70797-240-02) / 15 g in 1 TUBE (70797-240-15)
370797-240-031 TUBE in 1 CARTON (70797-240-03) / 15 g in 1 TUBE (70797-240-15)
470797-240-041 TUBE in 1 BLISTER PACK (70797-240-04) / 15 g in 1 TUBE (70797-240-15)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70797-240The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMENuby Soothing GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/25/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMETalbot's Pharmaceuticals Family Products, LLC.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC70797-240The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMENuby Soothing GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/21/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMETalbot's Pharmaceuticals Family Products, LLC.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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