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  4. NDC Product Code: 43846-0079 Bite, Bump And Rash Relief

NDC 43846-0079 Bite, Bump And Rash Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43846-0079?
  4. Bite, Bump And Rash Relief Uses
  5. Active Ingredients UNII Codes
  6. 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:
43846-0079
Proprietary Name:
Bite, Bump And Rash Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Peaceful Mountain, Inc.
Labeler Code:
43846
Product Label ID:
e158a743-160f-446e-a0ea-a2ce566d866f
Start Marketing Date: [9]
01-10-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43846-0079-1

Package Description: 57 g in 1 TUBE

Product Details

What is NDC 43846-0079?

The NDC code 43846-0079 is assigned by the FDA to the product Bite, Bump And Rash Relief 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 43846-0079-1 57 g in 1 tube . 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 Bite, Bump And Rash Relief?

May temporarily relieve itching, insect bites, poison ivy, rashes, eczema, hives, inflammation and irritated red skin.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve itching, insect bites, poison ivy, rashes, eczema, hives, inflammation and irritated red skin.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Which are Bite, Bump And Rash Relief UNII Codes?

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

  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
  • DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • ASTACUS ASTACUS (UNII: V0551986XQ)
  • ASTACUS ASTACUS (UNII: V0551986XQ) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)

Which are Bite, Bump And Rash Relief 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".