NDC 60986-1003 Allernest
Formicum Acidum,Lachesis Mutus,Luffa Operculata. Petroleum,Rhus Toxicodebdron,Aralai - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60986 - Marco Pharma International Llc.
- 60986-1003 - Allernest
Product Packages
NDC Code 60986-1003-3
Package Description: 50 mL in 1 BOTTLE, GLASS
NDC Code 60986-1003-4
Package Description: 100 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 60986-1003?
What are the uses for Allernest?
What are Allernest Active Ingredients?
- ARALIA RACEMOSA ROOT 4 [hp_X]/mL
- CARDIOSPERMUM HALICACABUM FLOWERING TOP 3 [hp_X]/mL
- FORMIC ACID 12 [hp_X]/mL
- GALPHIMIA GLAUCA FLOWERING TOP 4 [hp_X]/mL
- KEROSENE 6 [hp_X]/mL - A refined petroleum fraction used as a fuel as well as a solvent.
- LACHESIS MUTA VENOM 8 [hp_X]/mL
- LUFFA OPERCULATA FRUIT 6 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 4 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/mL
- URTICA DIOICA 4 [hp_X]/mL - A plant species of the genus Urtica, family URTICACEAE. Roots have been used to treat PROSTATIC HYPERPLASIA. Leaves are edible after the stinging quality is eliminated by brief heating.
Which are Allernest UNII Codes?
The UNII codes for the active ingredients in this product are:
- FORMIC ACID (UNII: 0YIW783RG1)
- FORMIC ACID (UNII: 0YIW783RG1) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- URTICA DIOICA (UNII: 710FLW4U46)
- URTICA DIOICA (UNII: 710FLW4U46) (Active Moiety)
- CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR)
- CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR) (Active Moiety)
Which are Allernest 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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".