70163-0007 NDC - OUTDOOR ALLERGIES (ACONITUM NAPELLUS, ADRENALINUM, ALLIUM CEPA, RAGWEED POLLEN, ARSENICUM IODATUM, MUGWORT POLLEN, MUSTARD POLLEN, LAMBS QUARTERS POLLEN, EUPHRASIA OFFICINALIS, HISTAMINUM HYDROCHLORICUM, PERENNIAL RYE GRASS POLLEN, ALFALFA POLLEN, TIMOTHY GRASS POLLEN, YELLOW DOCK POLLEN, SABADILLA, SILICEA, DANDELION POLLEN, RED CLOVER POLLEN, COCKLEBUR POLLEN)

Drug Information

Product NDC: 70163-0007
Proprietary Name: Outdoor Allergies
Non Proprietary Name: Aconitum Napellus, Adrenalinum, Allium Cepa, Ragweed Pollen, Arsenicum Iodatum, Mugwort Pollen, Mustard Pollen, Lambs Quarters Pollen, Euphrasia Officinalis, Histaminum Hydrochloricum, Perennial Rye Grass Pollen, Alfalfa Pollen, Timothy Grass Pollen, Yellow Dock Pollen, Sabadilla, Silicea, Dandelion Pollen, Red Clover Pollen, Cocklebur Pollen
Active Ingredient(s): 6 [hp_X]/1 ACONITUM NAPELLUS WHOLE; 12 [hp_X]/1 AMBROSIA ARTEMISIIFOLIA WHOLE; 6 [hp_X]/1 ARSENIC TRIIODIDE; 12 [hp_X]/1 ARTEMISIA VULGARIS POLLEN; 12 [hp_X]/1 BRASSICA RAPA SUBSP. OLEIFERA POLLEN; 12 [hp_X]/1 CHENOPODIUM ALBUM POLLEN; 6 [hp_X]/1 EPINEPHRINE; 6 [hp_X]/1 EUPHRASIA STRICTA; 12 [hp_X]/1 HISTAMINE DIHYDROCHLORIDE; 12 [hp_X]/1 LOLIUM PERENNE POLLEN; 12 [hp_X]/1 MEDICAGO SATIVA POLLEN; 6 [hp_X]/1 ONION; 12 [hp_X]/1 PHLEUM PRATENSE POLLEN; 12 [hp_X]/1 RUMEX CRISPUS POLLEN; 6 [hp_X]/1 SCHOENOCAULON OFFICINALE SEED; 6 [hp_X]/1 SILICON DIOXIDE; 12 [hp_X]/1 TARAXACUM OFFICINALE POLLEN; 12 [hp_X]/1 TRIFOLIUM PRATENSE POLLEN; 12 [hp_X]/1 XANTHIUM STRUMARIUM POLLEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; 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 Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Pollen Allergenic Extract [EPC]; Non-Standardized Pollen Allergenic Extract [EPC]; Non-Standardized Pollen Allergenic Extract [EPC]; Non-Standardized Pollen Allergenic Extract [EPC]; Non-Standardized Pollen Allergenic Extract [EPC]; Non-Standardized Pollen Allergenic Extract [EPC]; Non-Standardized Pollen Allergenic Extract [EPC]; Pollen [CS]; Pollen [CS]; Pollen [CS]; Pollen [CS]; Pollen [CS]; Pollen [CS]; Pollen [CS]; Pollen [CS]; Standardized Pollen Allergenic Extract [EPC]; Vegetable Proteins [CS]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	NaturalCare
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	70163-0007-1	1 BLISTER PACK in 1 CARTON (70163-0007-1) / 60 TABLET in 1 BLISTER PACK

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	70163-0007	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	Outdoor Allergies	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	Aconitum Napellus, Adrenalinum, Allium Cepa, Ragweed Pollen, Arsenicum Iodatum, Mugwort Pollen, Mustard Pollen, Lambs Quarters Pollen, Euphrasia Officinalis, Histaminum Hydrochloricum, Perennial Rye Grass Pollen, Alfalfa Pollen, Timothy Grass Pollen, Yellow Dock Pollen, Sabadilla, Silicea, Dandelion Pollen, Red Clover Pollen, Cocklebur Pollen	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	TABLET	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	NaturalCare	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	ACONITUM NAPELLUS WHOLE; AMBROSIA ARTEMISIIFOLIA WHOLE; ARSENIC TRIIODIDE; ARTEMISIA VULGARIS POLLEN; BRASSICA RAPA SUBSP. OLEIFERA POLLEN; CHENOPODIUM ALBUM POLLEN; EPINEPHRINE; EUPHRASIA STRICTA; HISTAMINE DIHYDROCHLORIDE; LOLIUM PERENNE POLLEN; MEDICAGO SATIVA POLLEN; ONION; PHLEUM PRATENSE POLLEN; RUMEX CRISPUS POLLEN; SCHOENOCAULON OFFICINALE SEED; SILICON DIOXIDE; TARAXACUM OFFICINALE POLLEN; TRIFOLIUM PRATENSE POLLEN; XANTHIUM STRUMARIUM POLLEN	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; 12; 6; 12; 12; 12; 6; 6; 12; 12; 12; 6; 12; 12; 6; 6; 12; 12; 12
ACTIVE INGRED UNIT	[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
PHARM CLASSES	Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], 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 Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Standardized Pollen Allergenic Extract [EPC], Vegetable Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]

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