66096-710 NDC - ALLERGY RELIEF (ALLIUM CEPA, APIS MELLIFICA, ARALIA RACEMOSA, BLATTA ORIENTALIS, BOVISTA, CARDUUS MARIANUS, CHELIDONIUM MAJUS, EUPHRASIA OFFICINALAS, GALPHIMIA GLAUCA, HEDERA HELIX, HYDRASTIS CANADENSIS, LUFFA OPERCULATA, NASTURTIUM AQUATICUM, OKOUBAKA, SABADILLA, SCROPHULARIA NODOSA, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE.)

Drug Information

Product NDC: 66096-710
Proprietary Name: Allergy Relief
Non Proprietary Name: Allium Cepa, Apis Mellifica, Aralia Racemosa, Blatta Orientalis, Bovista, Carduus Marianus, Chelidonium Majus, Euphrasia Officinalas, Galphimia Glauca, Hedera Helix, Hydrastis Canadensis, Luffa Operculata, Nasturtium Aquaticum, Okoubaka, Sabadilla, Scrophularia Nodosa, Solidago Virgaurea, Taraxacum Officinale.
Active Ingredient(s): 5 [hp_X]/59mL APIS MELLIFERA; 5 [hp_X]/59mL ARALIA RACEMOSA ROOT; 12 [hp_X]/59mL BLATTA ORIENTALIS; 3 [hp_X]/59mL CHELIDONIUM MAJUS; 8 [hp_X]/59mL EUPHRASIA STRICTA; 5 [hp_X]/59mL GALPHIMIA GLAUCA FLOWERING TOP; 5 [hp_X]/59mL GOLDENSEAL; 5 [hp_X]/59mL HEDERA HELIX FLOWERING TWIG; 5 [hp_X]/59mL LUFFA OPERCULATA FRUIT; 12 [hp_C]/59mL LYCOPERDON UTRIFORME FRUITING BODY; 3 [hp_X]/59mL MILK THISTLE; 3 [hp_X]/59mL NASTURTIUM OFFICINALE; 5 [hp_X]/59mL OKOUBAKA AUBREVILLEI BARK; 5 [hp_X]/59mL ONION; 5 [hp_X]/59mL SCHOENOCAULON OFFICINALE SEED; 3 [hp_X]/59mL SCROPHULARIA NODOSA; 5 [hp_X]/59mL SOLIDAGO VIRGAUREA FLOWERING TOP; 3 [hp_X]/59mL TARAXACUM OFFICINALE
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Insect Proteins [CS]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Insect Allergenic Extract [EPC]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]

Labeler Information

Field Name	Field Value
Labeler Name:	OHM PHARMA INC.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	6/2/2017

Package Information

No.	Package Code	Package Description	Billing Unit
1	66096-710-05	59 mL in 1 BOTTLE, SPRAY (66096-710-05)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	66096-710	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	Allergy Relief	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, Apis Mellifica, Aralia Racemosa, Blatta Orientalis, Bovista, Carduus Marianus, Chelidonium Majus, Euphrasia Officinalas, Galphimia Glauca, Hedera Helix, Hydrastis Canadensis, Luffa Operculata, Nasturtium Aquaticum, Okoubaka, Sabadilla, Scrophularia Nodosa, Solidago Virgaurea, Taraxacum Officinale.	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	6/2/2017	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	OHM PHARMA INC.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	APIS MELLIFERA; ARALIA RACEMOSA ROOT; BLATTA ORIENTALIS; CHELIDONIUM MAJUS; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; GOLDENSEAL; HEDERA HELIX FLOWERING TWIG; LUFFA OPERCULATA FRUIT; LYCOPERDON UTRIFORME FRUITING BODY; MILK THISTLE; NASTURTIUM OFFICINALE; OKOUBAKA AUBREVILLEI BARK; ONION; SCHOENOCAULON OFFICINALE SEED; SCROPHULARIA NODOSA; SOLIDAGO VIRGAUREA FLOWERING TOP; TARAXACUM OFFICINALE	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	5; 5; 12; 3; 8; 5; 5; 5; 5; 12; 3; 3; 5; 5; 5; 3; 5; 3
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_C]/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 CLASSES	Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Insect Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS]

Drug Information

Labeler Information

Package Information

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