NDC 43846-0014 Sciatic Rescue

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:
43846-0014
Proprietary Name:
Sciatic Rescue
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Peaceful Mountain, Inc.
Labeler Code:
43846
Start Marketing Date: [9]
08-24-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43846-0014-1

Package Description: 1814 g in 1 JUG

Product Details

What is NDC 43846-0014?

The NDC code 43846-0014 is assigned by the FDA to the product Sciatic Rescue which is product labeled by Peaceful Mountain, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43846-0014-1 1814 g in 1 jug . 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 Sciatic Rescue?

INDICATIONS: For temporary relief of sharp pain along the sciatic nerve, lower back and down the back of the legs.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Which are Sciatic Rescue UNII Codes?

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

  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW)
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (Active Moiety)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)

Which are Sciatic Rescue 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:

* Please review the disclaimer below.

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".