Cl-n

Emotional Health Booster

Vitality Works, Inc.
Human Otc Drug
NDC 64616-087

Cl-n also known as Emotional Health Booster is a human otc drug labeled by 'Vitality Works, Inc.'. National Drug Code (NDC) number for Cl-n is 64616-087. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Cl-n drug includes Aconitum Napellus - 6 [hp_X]/mL Ambergris - 12 [hp_X]/mL Ammi Visnaga Fruit - 10 [hp_X]/mL Apis Mellifera - 15 [hp_X]/mL Arnica Montana - 6 [hp_X]/mL Arsenic Trioxide - 12 [hp_X]/mL Baptisia Tinctoria Root - 12 [hp_X]/mL Barium Carbonate - 15 [hp_X]/mL Bellis Perennis - 10 [hp_X]/mL Berberis Vulgaris Root Bark - 10 [hp_X]/mL and more. The currest status of Cl-n drug is Active.

Drug Information:

Drug NDC:	64616-087
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.
Proprietary Name:	Cl-n
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Emotional Health Booster
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Vitality Works, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ACONITUM NAPELLUS - 6 [hp_X]/mL AMBERGRIS - 12 [hp_X]/mL AMMI VISNAGA FRUIT - 10 [hp_X]/mL APIS MELLIFERA - 15 [hp_X]/mL ARNICA MONTANA - 6 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL BAPTISIA TINCTORIA ROOT - 12 [hp_X]/mL BARIUM CARBONATE - 15 [hp_X]/mL BELLIS PERENNIS - 10 [hp_X]/mL BERBERIS VULGARIS ROOT BARK - 10 [hp_X]/mL Load more... BLACK MUSTARD SEED - 7 [hp_X]/mL CAUSTICUM - 5 [hp_X]/mL CHELIDONIUM MAJUS - 3 [hp_X]/mL CLEMATIS RECTA FLOWERING TOP - 30 [hp_X]/mL EUPATORIUM PERFOLIATUM FLOWERING TOP - 12 [hp_X]/mL FENNEL SEED - 12 [hp_X]/mL FERRUM PHOSPHORICUM - 10 [hp_X]/mL FRAXINUS AMERICANA BARK - 10 [hp_X]/mL LILIUM LANCIFOLIUM WHOLE FLOWERING - 5 [hp_X]/mL MARSDENIA CONDURANGO BARK - 17 [hp_X]/mL MATRICARIA RECUTITA - 7 [hp_X]/mL MERCURIC CHLORIDE - 15 [hp_X]/mL ORNITHOGALUM UMBELLATUM - 7 [hp_X]/mL PASSIFLORA INCARNATA FLOWERING TOP - 10 [hp_X]/mL SCROPHULARIA NODOSA - 15 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF - 7 [hp_X]/mL VERATRUM ALBUM ROOT - 7 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	08 Apr, 2013
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	16 Jan, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Vitality Works, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	U0NQ8555JD XTC0D02P6C 3UN285QN0C 7S82P3R43Z O80TY208ZW S7V92P67HO 5EF0HWI5WU 6P669D8HQ8 2HU33I03UY 1TH8Q20J0U Load more... 8LTY55LQ8D DD5FO1WKFU 7E889U5RNN 396421SP9F 1W0775VX6E G3QC02NIE6 91GQH8I5F7 0B24UR1O1S X67Z2963PI R23QIR6YBA G0R4UBI2ZZ 53GH7MZT1R 9NS3M2Y78S CLF5YFS11O 7H443NUB2T 6IO182RP7A QNS6W5US1Z
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Insect Venom Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Bee Venoms [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Bee Venoms [CS] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Increased IgG Production [PE] Standardized Insect Venom Allergenic Extract [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
64616-087-02	59 mL in 1 BOTTLE, DROPPER (64616-087-02)	08 Apr, 2013	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Cl-n

Emotional Health Booster

Liquid
Vitality Works, Inc.
NDC: 64616-087

Enc

Emotional Health Booster

Liquid
Vitality Works, Inc.
NDC: 64616-088

Op-p

Emotional Health Booster

Liquid
Vitality Works, Inc.
NDC: 64616-100

Purpose:

Cl-n eases depression, drowsiness, vertigo, malaise, headaches and confusion.

Product Elements:

Cl-n emotional health booster alcohol water aconitum napellus aconitum napellus ambergris ambergris ammi visnaga fruit ammi visnaga fruit apis mellifera apis mellifera arnica montana arnica montana arsenic trioxide arsenic cation (3+) baptisia tinctoria root baptisia tinctoria root barium carbonate barium cation bellis perennis bellis perennis berberis vulgaris root bark berberis vulgaris root bark causticum causticum matricaria recutita matricaria recutita chelidonium majus chelidonium majus clematis recta flowering top clematis recta flowering top marsdenia condurango bark marsdenia condurango bark eupatorium perfoliatum flowering top eupatorium perfoliatum flowering top ferrum phosphoricum ferrosoferric phosphate fennel seed fennel seed fraxinus americana bark fraxinus americana bark lilium lancifolium whole flowering lilium lancifolium whole flowering mercuric chloride mercuric cation ornithogalum umbellatum ornithogalum umbellatum passiflora incarnata flowering top passiflora incarnata flowering top toxicodendron pubescens leaf toxicodendron pubescens leaf scrophularia nodosa scrophularia nodosa black mustard seed black mustard seed veratrum album root veratrum album root

Indications and Usage:

Cl-n for the temporory relief of depression, drowsiness, vertigo, general systemic malaise, headaches and confusion.

Warnings:

Cl-n use only under the direction of a health care professional. do not use if tamper evident seal is broken or missing.

Dosage and Administration:

Cl-n orally 25 drops, 2 times per day or as indicated by a physician. children 12 and under use one half the adult dosage.

Package Label Principal Display Panel:

Cl-n label

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.