Ledum Combination 9257

Ledum Combination

Professional Complementary Health Formulas
Human Otc Drug
NDC 63083-9257

Ledum Combination 9257 also known as Ledum Combination is a human otc drug labeled by 'Professional Complementary Health Formulas'. National Drug Code (NDC) number for Ledum Combination 9257 is 63083-9257. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Ledum Combination 9257 drug includes Ammonium Cation - 8 [hp_X]/29.5mL Anhydrous Dibasic Calcium Phosphate - 10 [hp_X]/29.5mL Berberis Vulgaris Root Bark - 4 [hp_X]/29.5mL Black Cohosh - 4 [hp_X]/29.5mL Bos Taurus Bone Marrow - 8 [hp_X]/29.5mL Bos Taurus Intervertebral Disc - 8 [hp_X]/29.5mL Bovine Type Ii Collagen (tracheal Cartilage) - 8 [hp_X]/29.5mL Cinchona Officinalis Bark - 4 [hp_X]/29.5mL Citrullus Colocynthis Fruit Pulp - 6 [hp_X]/29.5mL Claviceps Purpurea Sclerotium - 6 [hp_X]/29.5mL and more. The currest status of Ledum Combination 9257 drug is Active.

Drug Information:

Drug NDC:	63083-9257
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:	Ledum Combination 9257
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	Ledum Combination
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix:	9257
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
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:	Ledum Combination
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Professional Complementary Health Formulas
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:	AMMONIUM CATION - 8 [hp_X]/29.5mL ANHYDROUS DIBASIC CALCIUM PHOSPHATE - 10 [hp_X]/29.5mL BERBERIS VULGARIS ROOT BARK - 4 [hp_X]/29.5mL BLACK COHOSH - 4 [hp_X]/29.5mL BOS TAURUS BONE MARROW - 8 [hp_X]/29.5mL BOS TAURUS INTERVERTEBRAL DISC - 8 [hp_X]/29.5mL BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) - 8 [hp_X]/29.5mL CINCHONA OFFICINALIS BARK - 4 [hp_X]/29.5mL CITRULLUS COLOCYNTHIS FRUIT PULP - 6 [hp_X]/29.5mL CLAVICEPS PURPUREA SCLEROTIUM - 6 [hp_X]/29.5mL Load more... CUPRIC ACETATE - 6 [hp_X]/29.5mL GONORRHEAL URETHRAL SECRETION HUMAN - 12 [hp_X]/29.5mL HORSE CHESTNUT - 6 [hp_X]/29.5mL MERCURIC OXIDE - 10 [hp_X]/29.5mL PICRIC ACID - 6 [hp_X]/29.5mL POTASSIUM CARBONATE - 6 [hp_X]/29.5mL PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE - 3 [hp_X]/29.5mL PULSATILLA MONTANA WHOLE - 6 [hp_X]/29.5mL RANUNCULUS BULBOSUS WHOLE - 4 [hp_X]/29.5mL RHODODENDRON TOMENTOSUM LEAFY TWIG - 4 [hp_X]/29.5mL SEPIA OFFICINALIS JUICE - 10 [hp_X]/29.5mL SILICON DIOXIDE - 6 [hp_X]/29.5mL SILVER - 10 [hp_X]/29.5mL SODIUM BORATE - 6 [hp_X]/29.5mL SULFUR - 30 [hp_X]/29.5mL SUS SCROFA ADRENAL GLAND - 10 [hp_X]/29.5mL ZINC - 10 [hp_X]/29.5mL
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:	15 Aug, 1984
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	08 May, 2026
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:	Professional Complementary Health Formulas
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.
UNII:	54S68520I4 L11K75P92J 1TH8Q20J0U K73E24S6X9 08X0K2M57P 0A04Z76C13 76TK29UQEZ S003A158SB 23H32AOH17 01G9XEA93N Load more... 39M11XPH03 9BZG9E3I8F 3C18L6RJAZ IY191986AO A49OS0F91S BQN1B9B9HA 36XQ854NWW 24K790T39B AEQ8NXJ0MB 877L01IZ0P QDL83WN8C2 ETJ7Z6XBU4 3M4G523W1G 91MBZ8H3QO 70FD1KFU70 398IYQ16YV J41CSQ7QDS
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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
63083-9257-1	29.5 mL in 1 BOTTLE, DROPPER (63083-9257-1)	15 Aug, 1985	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

Ledum Combination 9257

Ledum Combination

Liquid
Professional Complementary Health Formulas
NDC: 63083-9257

Purpose:

*claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Ledum combination 9257 ledum combination pseudognaphalium obtusifolium whole pseudognaphalium obtusifolium whole berberis vulgaris root bark berberis vulgaris root bark black cohosh black cohosh cinchona officinalis bark cinchona officinalis bark rhododendron tomentosum leafy twig rhododendron tomentosum leafy twig ranunculus bulbosus whole ranunculus bulbosus whole horse chestnut horse chestnut sodium borate borate ion citrullus colocynthis fruit pulp citrullus colocynthis fruit pulp cupric acetate cupric cation potassium carbonate carbonate ion picric acid picric acid pulsatilla montana whole pulsatilla montana whole claviceps purpurea sclerotium claviceps purpurea sclerotium silicon dioxide silicon dioxide ammonium cation ammonium cation bos taurus bone marrow bos taurus bone marrow bovine type ii collagen (tracheal cartilage) bovine type ii collagen (tracheal cartilage) bos taurus intervertebral disc bos taurus intervertebral disc sus scrofa adrenal gland sus scrofa adrenal gland silver silver anhydrous dibasic calcium phosphate anhydrous dibasic calcium phosphate mercuric oxide mercuric oxide sepia officinalis juice sepia officinalis juice zinc zinc gonorrheal urethral secretion human gonorrheal urethral secretion human sulfur sulfur alcohol water

Indications and Usage:

Indications for the temporary relief of mild joint, muscle, or back pain, stiffness, or tenderness.*

Warnings:

Warnings in case of overdose, get medical help or contact a poison control center right away. keep out of the reach of children. if pregnant or breastfeeding, ask a healthcare professional before use.

Dosage and Administration:

Directions place drops under tongue 30 minutes before/after meals. adults and children 12 years and over: take 10 drops up to 3 times per day. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Label est 1985 professional formulas complementary health ledum combination homeopathic remedy 1 fl. oz. (29.5 ml) label image

Further Questions:

Questions professional formulas po box 2034 lake oswego, or 97035

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.