NDC 70797-240 Nuby Soothing Gel

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70797-240
Proprietary Name:
Nuby Soothing Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
70797
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
08-25-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 70797-240?

The NDC code 70797-240 is assigned by the FDA to the product Nuby Soothing Gel which is product labeled by Talbot's Pharmaceuticals Family Products, Llc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 70797-240-01 1 tube in 1 blister pack / 15 g in 1 tube (70797-240-15), 70797-240-02 1 tube in 1 blister pack / 15 g in 1 tube (70797-240-15), 70797-240-03 1 tube in 1 carton / 15 g in 1 tube (70797-240-15). 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 Soothing Gel?

Temporarily relievesirritabilitycold chillsflu-like symptomsfeverbody achegeneral sorenessswollen glands

Which are Nuby Soothing Gel UNII Codes?

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

  • ARNICA MONTANA ROOT (UNII: MUE8Y11327)
  • ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • COSMOS SULPHUREUS FLOWERING TOP (UNII: WKB165X336)
  • COSMOS SULPHUREUS FLOWERING TOP (UNII: WKB165X336) (Active Moiety)
  • POTASSIUM CHLORIDE (UNII: 660YQ98I10)
  • POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)

Which are Nuby Soothing 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:

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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.

[8] What is the Marketing Category? - Product 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.

[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".