83027-0029 NDC - ASSIST (FOENICULUM VULGARE, AMMONIUM BROMATUM, FUCUS VESICULOSUS, LECITHIN (DERIVED FROM EGG), CAPSICUM ANNUUM, GALIUM APARINE, HYPOTHALAMUS SUIS, KALI BICHROMICUM, LAC DEFLORATUM (NSPC), PHYTOLACCA DECANDRA, THYROIDINUM (BOVINE), PITUITARUM POSTERIUM (BOVINE), ANTIMONIUM CRUDUM, ARGENTUM METALLICUM, CALCAREA CARBONICA, ADRENALINUM, PHOSPHORUS)

Drug Information

Product NDC: 83027-0029
Proprietary Name: Assist
Non Proprietary Name: Foeniculum Vulgare, Ammonium Bromatum, Fucus Vesiculosus, Lecithin (Derived From Egg), Capsicum Annuum, Galium Aparine, Hypothalamus Suis, Kali Bichromicum, Lac Defloratum (NSPC), Phytolacca Decandra, Thyroidinum (Bovine), Pituitarum Posterium (Bovine), Antimonium Crudum, Argentum Metallicum, Calcarea Carbonica, Adrenalinum, Phosphorus
Active Ingredient(s): 3 [hp_X]/mL AMMONIUM BROMIDE; 9 [hp_X]/mL ANTIMONY TRISULFIDE; 8 [hp_X]/mL BOS TAURUS PITUITARY GLAND, POSTERIOR; 6 [hp_X]/mL CAPSICUM; 4 [hp_X]/mL EGG PHOSPHOLIPIDS; 12 [hp_X]/mL EPINEPHRINE; 2 [hp_X]/mL FOENICULUM VULGARE FRUIT; 3 [hp_X]/mL FUCUS VESICULOSUS; 6 [hp_X]/mL GALIUM APARINE WHOLE; 9 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 12 [hp_X]/mL PHOSPHORUS; 6 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 6 [hp_X]/mL POTASSIUM DICHROMATE; 9 [hp_X]/mL SILVER; 6 [hp_X]/mL SKIM MILK; 6 [hp_X]/mL SUS SCROFA PITUITARY GLAND; 6 [hp_X]/mL THYROID, BOVINE
Administration Route(s): ORAL
Dosage Form(s): SPRAY
Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Allergens [CS]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; 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:	3/29/2023

Package Information

No.	Package Code	Package Description	Billing Unit
1	83027-0029-1	60 mL in 1 BOTTLE, SPRAY (83027-0029-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	83027-0029	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	Assist	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	Foeniculum Vulgare, Ammonium Bromatum, Fucus Vesiculosus, Lecithin (Derived From Egg), Capsicum Annuum, Galium Aparine, Hypothalamus Suis, Kali Bichromicum, Lac Defloratum (NSPC), Phytolacca Decandra, Thyroidinum (Bovine), Pituitarum Posterium (Bovine), Antimonium Crudum, Argentum Metallicum, Calcarea Carbonica, Adrenalinum, Phosphorus	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	SPRAY	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	3/29/2023	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	AMMONIUM BROMIDE; ANTIMONY TRISULFIDE; BOS TAURUS PITUITARY GLAND, POSTERIOR; CAPSICUM; EGG PHOSPHOLIPIDS; EPINEPHRINE; FOENICULUM VULGARE FRUIT; FUCUS VESICULOSUS; GALIUM APARINE WHOLE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM DICHROMATE; SILVER; SKIM MILK; SUS SCROFA PITUITARY GLAND; THYROID, BOVINE	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	3; 9; 8; 6; 4; 12; 2; 3; 6; 9; 12; 6; 6; 9; 6; 6; 6
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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
PHARM CLASSES	Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]

Drug Information

Labeler Information

Package Information

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