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NDC 57955-9997 Allergy Relief Indoor And Outdoor

Allium Cepa,Ambrosia Artemisiaefolia,Arsenicum Album,Arum Triphyllum,Arundo - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-9997?
  4. Active Ingredients
  5. Pharmacologic Classes

Product Information

This code was recently added to the official NDC directory and the product has entered commercial distribution.

Get all the details for National Drug Code (NDC) 57955-9997 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
57955-9997
Proprietary Name:
Allergy Relief Indoor And Outdoor
Non-Proprietary Name: [1]
Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Album, Arum Triphyllum, Arundo Mauritanica, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrochloricum, Kali Bichromicum, Naphthalinum, Natrum Muriaticum, Sabadilla, Solidago Virgaurea, Sticta Pulmonaria, Sulphur, Trifolium Pratense, And Wyethia Helenioides.
Substance Name: [2]
Ambrosia Artemisiifolia Whole; Arisaema Triphyllum Root; Arsenic Trioxide; Arundo Pliniana Root; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Lobaria Pulmonaria; Naphthalene; Onion; Potassium Dichromate; Schoenocaulon Officinale Seed; Sodium Chloride; Solidago Virgaurea Flowering Top; Sulfur; Trifolium Pratense Flower; Wyethia Helenioides Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
10-20-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
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Product Details

What is NDC 57955-9997?

The NDC code 57955-9997 is assigned by the FDA to the product Allergy Relief Indoor And Outdoor which is a human over the counter drug product labeled by King Bio Inc.. The generic name of Allergy Relief Indoor And Outdoor is allium cepa, ambrosia artemisiaefolia, arsenicum album, arum triphyllum, arundo mauritanica, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, kali bichromicum, naphthalinum, natrum muriaticum, sabadilla, solidago virgaurea, sticta pulmonaria, sulphur, trifolium pratense, and wyethia helenioides.. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 57955-9997-2 59 ml in 1 bottle, spray . 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 Allergy Relief Indoor And Outdoor Active Ingredients?

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.

Which are the Pharmacologic Classes for Allergy Relief Indoor And Outdoor?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product Footnotes

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".