NDC 64616-087 Cl-n

Emotional Health Booster

NDC Product Code 64616-087

NDC Product Information

Cl-n with NDC 64616-087 is a a human over the counter drug product labeled by Vitality Works, Inc.. The generic name of Cl-n is emotional health booster. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Vitality Works, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
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.

Cl-n Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • 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
  • CAUSTICUM 5 [hp_X]/mL
  • MATRICARIA RECUTITA 7 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • CLEMATIS RECTA FLOWERING TOP 30 [hp_X]/mL
  • MARSDENIA CONDURANGO BARK 17 [hp_X]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 12 [hp_X]/mL
  • FERRUM PHOSPHORICUM 10 [hp_X]/mL
  • FENNEL SEED 12 [hp_X]/mL
  • FRAXINUS AMERICANA BARK 10 [hp_X]/mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 5 [hp_X]/mL
  • MERCURIC CHLORIDE 15 [hp_X]/mL
  • ORNITHOGALUM UMBELLATUM 7 [hp_X]/mL
  • PASSIFLORA INCARNATA FLOWERING TOP 10 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 7 [hp_X]/mL
  • SCROPHULARIA NODOSA 15 [hp_X]/mL
  • BLACK MUSTARD SEED 7 [hp_X]/mL
  • VERATRUM ALBUM ROOT 7 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Vitality Works, Inc.
Labeler Code: 64616
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
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.

Start Marketing Date: 04-08-2013 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Cl-n Product Label Images

Cl-n Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Cl-N

Aconitum Napellus 6X                      Berberis Vuylgaris 10X                          Fraxinus Americana 10X


Ambra Grisea 12X                            Causticum 5X                                        Lilium Tigrinum 5X


Ammi Visnaga 10X                           Chamomilla 7X                                      Mercurius Corrosivus 15X


Apis Mellifica 3X, 15X                       Chilidonium Majus 3X                            Ornithogalum Umbellatum 7X


Arnica Montana 6X                          Clematis Erecta 10X, 15X, 30X              Passiblora Incarnata 10X


Arsenicum Album 8X, 12X                Condurango 17X                                   Rhus Toxicodendron 7X


Baptisia Tinctoria 12X                      Eupatorium Perfoliatum 6X, 12X           Scrophularia Nodosa 15X


Baryta Carbonica 15X                     Ferrum Phosphoricum 10X                     Sinapsis Nigra 7X


Bellis Perennis 10X                         Foeniculum Vulgare 6X, 12X                  Veratum Album 7X

Alcohol, Purified Water

Use only under the direction of a health care professional. Do not use if tamper evident seal is broken or missing.

Keep out of reach of children. In case of overdose, get meidcal help or contact a Poison Control Center right away.

For the temporory relief of depression, drowsiness, vertigo, general systemic malaise, headaches and confusion.

Orally 25 drops, 2 times per day or as indicated by a physician. Children 12 and under use one half the adult dosage.

Eases depression, drowsiness, vertigo, malaise, headaches and confusion.

* Please review the disclaimer below.

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