83027-0142 NDC - PINEAL LIQUESCENCE (VALERIANA OFFICINALIS, HYDROCOTYLE ASIATICA, MELATONIN, CEREBRUM SUIS, HYPOTHALAMUS SUIS, PINEAL GLAND (SUIS), SCUTELLARIA LATERIFLORA, STELLARIA MEDIA, CALCAREA CARBONICA, ZINCUM METALLICUM, AURUM METALLICUM, DOPAMINE (HYDROCHLORIDE), SEROTONIN (HYDROCHLORIDE), MAGNESIA MURIATICA)

Drug Information

Product NDC: 83027-0142
Proprietary Name: Pineal Liquescence
Non Proprietary Name: Valeriana Officinalis, Hydrocotyle Asiatica, Melatonin, Cerebrum Suis, Hypothalamus Suis, Pineal Gland (Suis), Scutellaria Lateriflora, Stellaria Media, Calcarea Carbonica, Zincum Metallicum, Aurum Metallicum, Dopamine (Hydrochloride), Serotonin (Hydrochloride), Magnesia Muriatica
Active Ingredient(s): 3 [hp_X]/mL CENTELLA ASIATICA WHOLE; 12 [hp_X]/mL DOPAMINE HYDROCHLORIDE; 12 [hp_X]/mL GOLD; 15 [hp_X]/mL MAGNESIUM CHLORIDE; 3 [hp_X]/mL MELATONIN; 9 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 6 [hp_X]/mL SCUTELLARIA LATERIFLORA WHOLE; 12 [hp_X]/mL SEROTONIN HYDROCHLORIDE; 6 [hp_X]/mL STELLARIA MEDIA; 6 [hp_X]/mL SUS SCROFA CEREBRUM; 6 [hp_X]/mL SUS SCROFA HYPOTHALAMUS; 6 [hp_X]/mL SUS SCROFA PINEAL GLAND; 2 [hp_X]/mL VALERIAN; 9 [hp_X]/mL ZINC
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): Allergens [CS]; Calculi Dissolution Agent [EPC]; Catecholamine [EPC]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Standardized Chemical Allergen [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

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:	7/24/2024

Package Information

No.	Package Code	Package Description	Billing Unit
1	83027-0142-1	120 mL in 1 BOTTLE, GLASS (83027-0142-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	83027-0142	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	Pineal 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	Valeriana Officinalis, Hydrocotyle Asiatica, Melatonin, Cerebrum Suis, Hypothalamus Suis, Pineal Gland (Suis), Scutellaria Lateriflora, Stellaria Media, Calcarea Carbonica, Zincum Metallicum, Aurum Metallicum, Dopamine (Hydrochloride), Serotonin (Hydrochloride), Magnesia Muriatica	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	7/24/2024	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	CENTELLA ASIATICA WHOLE; DOPAMINE HYDROCHLORIDE; GOLD; MAGNESIUM CHLORIDE; MELATONIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SCUTELLARIA LATERIFLORA WHOLE; SEROTONIN HYDROCHLORIDE; STELLARIA MEDIA; SUS SCROFA CEREBRUM; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PINEAL GLAND; VALERIAN; ZINC	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; 12; 12; 15; 3; 9; 6; 12; 6; 6; 6; 6; 2; 9
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
PHARM CLASSES	Allergens [CS], Calculi Dissolution Agent [EPC], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Drug Information

Labeler Information

Package Information

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