83027-0301 NDC - POLLEN AND DANDER LIQUESCENCE (ALLIUM CEPA, EUPHRASIA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), SABADILLA, AMBROSIA ARTEMISIAEFOLIA, APIS MELLIFICA, GALIUM APARINE, GLANDULA SUPRARENALIS (BOVINE), HEPAR (BOVINE), HYDRASTIS CANADENSIS, ADRENALINUM, HISTAMINUM HYDROCHLORICUM, STICTA PULMONARIA)

Drug Information

Product NDC: 83027-0301
Proprietary Name: Pollen and Dander Liquescence
Non Proprietary Name: Allium Cepa, Euphrasia Officinalis, Echinacea (Angustifolia), Sabadilla, Ambrosia Artemisiaefolia, Apis Mellifica, Galium Aparine, Glandula Suprarenalis (Bovine), Hepar (Bovine), Hydrastis Canadensis, Adrenalinum, Histaminum Hydrochloricum, Sticta Pulmonaria
Active Ingredient(s): 6 [hp_X]/mL AMBROSIA ARTEMISIIFOLIA WHOLE; 6 [hp_X]/mL APIS MELLIFERA; 6 [hp_X]/mL BEEF LIVER; 6 [hp_X]/mL BOS TAURUS ADRENAL GLAND; 2 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 12 [hp_X]/mL EPINEPHRINE; 1 [hp_X]/mL EUPHRASIA STRICTA; 6 [hp_X]/mL GALIUM APARINE WHOLE; 6 [hp_X]/mL GOLDENSEAL; 12 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE; 12 [hp_X]/mL LOBARIA PULMONARIA; 1 [hp_X]/mL ONION; 4 [hp_X]/mL SCHOENOCAULON OFFICINALE SEED
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Meat Proteins [EXT]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	Nutritional Specialties, Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	2/23/2026

Package Information

No.	Package Code	Package Description	Billing Unit
1	83027-0301-1	120 mL in 1 BOTTLE, GLASS (83027-0301-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	83027-0301	The 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 NAME	HUMAN OTC DRUG	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.
PROPRIETARY NAME	Pollen and Dander Liquescence	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	Allium Cepa, Euphrasia Officinalis, Echinacea (Angustifolia), Sabadilla, Ambrosia Artemisiaefolia, Apis Mellifica, Galium Aparine, Glandula Suprarenalis (Bovine), Hepar (Bovine), Hydrastis Canadensis, Adrenalinum, Histaminum Hydrochloricum, Sticta Pulmonaria	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	LIQUID	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	2/23/2026	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	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.
LABELER NAME	Nutritional Specialties, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	AMBROSIA ARTEMISIIFOLIA WHOLE; APIS MELLIFERA; BEEF LIVER; BOS TAURUS ADRENAL GLAND; ECHINACEA ANGUSTIFOLIA WHOLE; EPINEPHRINE; EUPHRASIA STRICTA; GALIUM APARINE WHOLE; GOLDENSEAL; HISTAMINE DIHYDROCHLORIDE; LOBARIA PULMONARIA; ONION; SCHOENOCAULON OFFICINALE SEED	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.
ACTIVE NUMERATOR STRENGTH	6; 6; 6; 6; 2; 12; 1; 6; 6; 12; 12; 1; 4
ACTIVE INGRED UNIT	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
PHARM CLASSES	Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Meat Proteins [EXT], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]

Drug Information

Labeler Information

Package Information

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