57955-9997 NDC - ALLERGY RELIEF INDOOR AND OUTDOOR (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.)

Drug Information

  • Product NDC: 57955-9997
  • Proprietary Name: Allergy Relief Indoor and Outdoor
  • Non Proprietary Name: 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.
  • Active Ingredient(s): 10 [hp_X]/59mL AMBROSIA ARTEMISIIFOLIA WHOLE; 10 [hp_X]/59mL ARISAEMA TRIPHYLLUM ROOT; 10 [hp_X]/59mL ARSENIC TRIOXIDE; 10 [hp_X]/59mL ARUNDO PLINIANA ROOT; 10 [hp_X]/59mL EUPHRASIA STRICTA; 10 [hp_X]/59mL GALPHIMIA GLAUCA FLOWERING TOP; 10 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE; 10 [hp_X]/59mL LOBARIA PULMONARIA; 10 [hp_X]/59mL NAPHTHALENE; 10 [hp_X]/59mL ONION; 10 [hp_X]/59mL POTASSIUM DICHROMATE; 10 [hp_X]/59mL SCHOENOCAULON OFFICINALE SEED; 10 [hp_X]/59mL SODIUM CHLORIDE; 10 [hp_X]/59mL SOLIDAGO VIRGAUREA FLOWERING TOP; 10 [hp_X]/59mL SULFUR; 10 [hp_X]/59mL TRIFOLIUM PRATENSE FLOWER; 10 [hp_X]/59mL WYETHIA HELENIOIDES ROOT
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: King Bio Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/20/2025

Package Information

No. Package Code Package Description Billing Unit
157955-9997-259 mL in 1 BOTTLE, SPRAY (57955-9997-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-9997The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEAllergy Relief Indoor and OutdoorThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAllium 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 non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/20/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEKing Bio Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMBROSIA 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 ROOTAn 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.
ACTIVE NUMERATOR STRENGTH10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Vegetable Proteins [CS] 

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This page was last updated on: 12/6/2025

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