NDC 55714-2386 Appetite - Craving Control

Anacardium Orientale, Antimon.crud., Arg. Nit., Berber. Vulg., Bryonia, Chelidonium Majus, Digitalis, Graphites, Humulus,iris Versicolor, Kali Carb., Lycopodium, Nat. Carb.,nat. Sulphuricum, Nux Vom., Pulsatilla, Rhus. Toxicodendron, Scutellaria Lateriflora, Sepia,stramonium, Chamomilla, Passiflora, Valeriana.

NDC Product Code 55714-2386

NDC Code: 55714-2386

Proprietary Name: Appetite - Craving Control What is the Proprietary Name?
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: Anacardium Orientale, Antimon.crud., Arg. Nit., Berber. Vulg., Bryonia, Chelidonium Majus, Digitalis, Graphites, Humulus,iris Versicolor, Kali Carb., Lycopodium, Nat. Carb.,nat. Sulphuricum, Nux Vom., Pulsatilla, Rhus. Toxicodendron, Scutellaria Lateriflora, Sepia,stramonium, Chamomilla, Passiflora, Valeriana. What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 55714 - Newton Laboratories, Inc.
    • 55714-2386 - Appetite - Craving Control

NDC 55714-2386-0

Package Description: .5 mL in 1 BOTTLE, GLASS

NDC 55714-2386-1

Package Description: 30 mL in 1 BOTTLE, GLASS

NDC 55714-2386-2

Package Description: 50 mL in 1 BOTTLE, GLASS

NDC Product Information

Appetite - Craving Control with NDC 55714-2386 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Appetite - Craving Control is anacardium orientale, antimon.crud., arg. nit., berber. vulg., bryonia, chelidonium majus, digitalis, graphites, humulus,iris versicolor, kali carb., lycopodium, nat. carb.,nat. sulphuricum, nux vom., pulsatilla, rhus. toxicodendron, scutellaria lateriflora, sepia,stramonium, chamomilla, passiflora, valeriana.. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, 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.

Appetite - Craving Control 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.

  • SEMECARPUS ANACARDIUM JUICE 15 [hp_X]/mL
  • ANTIMONY TRISULFIDE 15 [hp_X]/mL
  • SILVER NITRATE 15 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • DIGITALIS 15 [hp_X]/mL
  • GRAPHITE 15 [hp_X]/mL
  • HOPS 15 [hp_X]/mL
  • IRIS VERSICOLOR ROOT 15 [hp_X]/mL
  • POTASSIUM CARBONATE 15 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mL
  • SODIUM CARBONATE 15 [hp_X]/mL
  • SODIUM SULFATE 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • PULSATILLA VULGARIS 15 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 15 [hp_X]/mL
  • SCUTELLARIA LATERIFLORA 15 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 15 [hp_X]/mL
  • DATURA STRAMONIUM 15 [hp_X]/mL
  • MATRICARIA RECUTITA 6 [hp_X]/mL
  • PASSIFLORA INCARNATA FLOWERING TOP 6 [hp_X]/mL
  • VALERIAN 6 [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)

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: Newton Laboratories, Inc.
Labeler Code: 55714
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: 10-29-2018 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.

Appetite - Craving Control Product Label Images

Appetite - Craving Control 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

Indications & Usage Section

Formulated for associated symptoms such as grief, despondency, difficult concentration, iritability, oversensitity and prolonged sadness.

Warnings Section

WARNINGS: Keep out of reach of children. Do not use, if taper-evident seal is broken or missing. If symptoms persist for more than a few days, consult a doctor. If
pregnant or breast-feeding, ask a doctord before use.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

Otc - Pregnancy Or Breast Feeding Section

If
pregnant or breast-feeding, ask a doctor before use.

Questions Section

Newtonlabs.net ~ Questions? 800.448.7256
Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA30013

Inactive Ingredient Section

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

Otc - Purpose Section

Formulated for associated symptoms such as overeating, cravings, fatigue and emotional discomfort.

Otc - Active Ingredient Section

Equal parts of Chamomilla 6x, Passiflora 6x, Valeriana 6x, Anacardium orientale 15x, Antimon.crud. 15x, Arg. nit. 15x, Berber. vulg. 15x, Bryonia 15x,Chelidonium maj.15x, Digitalis 15x, Graphites 15x, Humulus 15x,Iris vers. 15x, Kali carb. 15x, Lycopodium 15x, Nat. carb. 15x ,Nat. sulphuricum 15x, Nux vom. 15x, Pulsatilla 15x, Rhus tox.15x, Scutellaria lateriflora 15x, Sepia 15x, Stramonium 15x.

Dosage & Administration Section

Directions: Ages 12 and up, take 6 drops by mouth (ages 6 to 11, give 3 drops) as needed or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

* Please review the disclaimer below.

Previous Code
55714-2385
Next Code
55714-2387