NDC 35378-0006 Control Remedy Water

Anacardium Orientale, Antimon. Crud., Arg. Nit., Berber. Vulg., Bryonia, Chelidonium Majus, Digitalis, Graphites, Humulus, Iris Versicolor,

NDC Product Code 35378-0006

NDC Code: 35378-0006

Proprietary Name: Control Remedy Water 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, 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

  • 35378 - Georgetown Health, Llc Dba Essentialife
    • 35378-0006 - Control Remedy Water

NDC 35378-0006-2

Package Description: 7 CYLINDER in 1 CONTAINER > 1000 mg in 1 CYLINDER

NDC 35378-0006-3

Package Description: 1 CYLINDER in 1 CONTAINER > 1000 mg in 1 CYLINDER

NDC Product Information

Control Remedy Water with NDC 35378-0006 is a a human over the counter drug product labeled by Georgetown Health, Llc Dba Essentialife. The generic name of Control Remedy Water is anacardium orientale, antimon. crud., arg. nit., berber. vulg., bryonia, chelidonium majus, digitalis, graphites, humulus, iris versicolor,. The product's dosage form is solution and is administered via oral form.

Labeler Name: Georgetown Health, Llc Dba Essentialife

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.

Control Remedy Water 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]/mg
  • ANTIMONY TRISULFIDE 15 [hp_X]/mg
  • SILVER NITRATE 15 [hp_X]/mg
  • BERBERIS VULGARIS ROOT BARK 15 [hp_X]/mg
  • BRYONIA ALBA ROOT 15 [hp_X]/mg
  • CHELIDONIUM MAJUS 15 [hp_X]/mg
  • DIGITALIS 15 [hp_X]/mg
  • GRAPHITE 15 [hp_X]/mg
  • HOPS 15 [hp_X]/mg
  • IRIS VERSICOLOR ROOT 15 [hp_X]/mg
  • POTASSIUM CARBONATE 15 [hp_X]/mg
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mg
  • SODIUM CARBONATE 15 [hp_X]/mg
  • SODIUM SULFATE 15 [hp_X]/mg
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mg
  • PULSATILLA VULGARIS 15 [hp_X]/mg
  • TOXICODENDRON PUBESCENS LEAF 15 [hp_X]/mg
  • SCUTELLARIA LATERIFLORA 15 [hp_X]/mg
  • SEPIA OFFICINALIS JUICE 15 [hp_X]/mg
  • DATURA STRAMONIUM 15 [hp_X]/mg
  • MATRICARIA RECUTITA 3 [hp_X]/mg
  • PASSIFLORA INCARNATA FLOWER 3 [hp_X]/mg
  • VALERIAN 3 [hp_X]/mg

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.

  • STARCH, CORN (UNII: O8232NY3SJ)
  • SUCROSE (UNII: C151H8M554)

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: Georgetown Health, Llc Dba Essentialife
Labeler Code: 35378
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: 07-01-2012 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.

Control Remedy Water Product Label Images

Control Remedy Water 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

Active Ingredients

Anacardium orientale15xAntimonium crudum15xArgentum nitricum15xBerberis vulgaris15xBryonia15xChelidonium majus15xDigitalis purpurea15xGraphites15xHumulus lupulus15xIris versicolor15xKali carbonicum15xLycopodium clavatum15xNatrum carbonicum15xNatrum sulphuricum15xNux vomica15xPulsatilla15xRhus toxicodendron15xScutellaria laterifolia15xSepia15xStramonium15xChamomilla3xPassiflora incarnata3xValeriana officinalis3x

Purpose

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

Uses

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

Warnings

Do not use if tamper-evident package seal is broken or missing.  Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.  Keep out of reach of children.

Directions

Ages 12 and up. Remedy Water® homepathic pellets are dispersed via the PowerCap® apparatus. Firmly press PowerCap® dome to release pellets into the bottle of water and shake well. Remedy Water® pellets may not dissolve completely. Drink within four hours. Avoid storing or washing where temperatures may exceed 140 degrees.

Inactive Ingredients

USP/NF neutral pellets (.07% gluten-free, non-GMO, beet-derived sucrose, .03% gluten-free, non-GMO maize starch in 500 ml water)

Other Information

Avoid storing in areas where temperatures may exceed 140 degrees.

Questions?

1.866.777.1277www.RemedyWater.com

* Please review the disclaimer below.

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