73399-002 NDC - FORMULA 2 (AGNUS CASTUS, ALPHA LIPOICUM ACIDUM, ANDROSTERONE 1 DHEA, CALCAREA CARBONICA,CINCHONA OFFICINALIS, CYNARA SCOLYMUS, DOPAMINE HYDROCHLORIDE, HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, OXYTOCIN ACETATE, QUERCETIN, SARCOLACTICUM, SEROTONIN, IGNATIA AMARA, TILIROSIDE, UBIQUINONE, VALERIANA OFFICINALIS,)

Drug Information

Product NDC: 73399-002
Proprietary Name: Formula 2
Non Proprietary Name: Agnus Castus, Alpha lipoicum acidum, Androsterone 1 DHEA, Calcarea carbonica,Cinchona officinalis, Cynara Scolymus, Dopamine Hydrochloride, Hydrastis canadensis, Lycopodium clavatum, Oxytocin acetate, Quercetin, Sarcolacticum, Serotonin, Ignatia amara, Tiliroside, Ubiquinone, Valeriana Officinalis,
Active Ingredient(s): 30 [hp_X]/30mL ALPHA LIPOIC ACID; 30 [hp_X]/30mL ANDROSTERONE; 60 [hp_X]/30mL CHASTE TREE FRUIT; 30 [hp_X]/30mL CINCHONA OFFICINALIS BARK; 60 [hp_X]/30mL CYNARA SCOLYMUS LEAF; 30 [hp_X]/30mL GOLDENSEAL; 30 [hp_C]/30mL LACTIC ACID, L-; 30 [hp_X]/30mL LYCOPODIUM CLAVATUM SPORE; 30 [hp_C]/30mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 30 [hp_X]/30mL QUERCETIN; 30 [hp_C]/30mL SEROTONIN; 30 [hp_C]/30mL STRYCHNOS IGNATII SEED; 30 [hp_X]/30mL TILIROSIDE; 30 [hp_X]/30mL UBIDECARENONE; 60 [hp_X]/30mL VALERIAN
Administration Route(s): ORAL
Dosage Form(s): LIQUID

Labeler Information

Field Name	Field Value
Labeler Name:	20Lighter, LLC.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	1/30/2020

Package Information

No.	Package Code	Package Description	Billing Unit
1	73399-002-30	30 mL in 1 BOTTLE (73399-002-30)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	73399-002	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	Formula 2	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	Agnus Castus, Alpha lipoicum acidum, Androsterone 1 DHEA, Calcarea carbonica,Cinchona officinalis, Cynara Scolymus, Dopamine Hydrochloride, Hydrastis canadensis, Lycopodium clavatum, Oxytocin acetate, Quercetin, Sarcolacticum, Serotonin, Ignatia amara, Tiliroside, Ubiquinone, Valeriana Officinalis,	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	1/30/2020	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	20Lighter, LLC.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	ALPHA LIPOIC ACID; ANDROSTERONE; CHASTE TREE FRUIT; CINCHONA OFFICINALIS BARK; CYNARA SCOLYMUS LEAF; GOLDENSEAL; LACTIC ACID, L-; LYCOPODIUM CLAVATUM SPORE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; QUERCETIN; SEROTONIN; STRYCHNOS IGNATII SEED; TILIROSIDE; UBIDECARENONE; VALERIAN	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	30; 30; 60; 30; 60; 30; 30; 30; 30; 30; 30; 30; 30; 30; 60
ACTIVE INGRED UNIT	[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL

Drug Information

Labeler Information

Package Information

NDC Record

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