NDC 44911-0067 Bone Repair HP

Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Hekla Lava, Hydrofluoricum Acidum, Magnesia Phosphorica, Rhus Tox, Ruta Graveolens, Silicea, Symphytum Officinale

NDC Product Code 44911-0067

NDC CODE: 44911-0067

Proprietary Name: Bone Repair HP 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: Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Hekla Lava, Hydrofluoricum Acidum, Magnesia Phosphorica, Rhus Tox, Ruta Graveolens, Silicea, Symphytum Officinale 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

  • 44911 - Energique, Inc.

NDC 44911-0067-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bone Repair HP with NDC 44911-0067 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Bone Repair HP is calcarea carbonica, calcarea fluorica, calcarea phosphorica, hekla lava, hydrofluoricum acidum, magnesia phosphorica, rhus tox, ruta graveolens, silicea, symphytum officinale. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, 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.

Bone Repair HP 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.

  • CALCIUM FLUORIDE 30 [hp_X]/mL
  • COMFREY ROOT 30 [hp_X]/mL
  • HEKLA LAVA 30 [hp_X]/mL
  • HYDROFLUORIC ACID 30 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 30 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL
  • RUTA GRAVEOLENS FLOWERING TOP 30 [hp_X]/mL
  • SILICON DIOXIDE 30 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 30 [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.

  • WATER (UNII: 059QF0KO0R)
  • 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.
  • 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: Energique, Inc.
Labeler Code: 44911
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: 02-20-2013 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: 12-31-2020 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.

Bone Repair HP Product Label Images

Bone Repair HP 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:

Calcarea Carbonica 30X, Calcarea Fluorica 30X, Calcarea Phosphorica 30X, Hekla Lava 30X, Hydrofluoricum Acidum 30X, Magnesia Phosphorica 30X, Rhus Tox 30X, Ruta Graveolens 30X, Silicea 30X, Symphytum Officinale 30X.

Indications:

For temporary relief of symptoms of chronic inflammation of the back and bone injury.**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms of chronic inflammation of the back and bone injury.**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breast-feeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Directions:

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 20% Ethanol.

Keep Out Of Reach Of Children:

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

Questions:

Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579    800-869-8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYBONE REPAIR HP1 fl. oz. (30 ml)

* Please review the disclaimer below.