Echinacea Combination 9222

Echinacea Combination

Professional Complementary Health Formulas
Human Otc Drug
NDC 63083-9222

Echinacea Combination 9222 also known as Echinacea Combination is a human otc drug labeled by 'Professional Complementary Health Formulas'. National Drug Code (NDC) number for Echinacea Combination 9222 is 63083-9222. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Echinacea Combination 9222 drug includes Aconitum Napellus Whole - 3 [hp_X]/29.5mL Aristolochia Clematitis Root - 12 [hp_X]/29.5mL Arnica Montana Whole - 4 [hp_X]/29.5mL Arsenic Trioxide - 8 [hp_X]/29.5mL Baptisia Tinctoria Whole - 4 [hp_X]/29.5mL Bryonia Alba Root - 6 [hp_X]/29.5mL Calcium Sulfide - 10 [hp_X]/29.5mL Cortisone Acetate - 13 [hp_X]/29.5mL Echinacea Angustifolia Whole - 2 [hp_X]/29.5mL Eupatorium Perfoliatum Flowering Top - 6 [hp_X]/29.5mL and more. The currest status of Echinacea Combination 9222 drug is Active.

Drug Information:

Drug NDC:	63083-9222
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:	Echinacea Combination 9222
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	Echinacea Combination
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix:	9222
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:	Echinacea 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:	ACONITUM NAPELLUS WHOLE - 3 [hp_X]/29.5mL ARISTOLOCHIA CLEMATITIS ROOT - 12 [hp_X]/29.5mL ARNICA MONTANA WHOLE - 4 [hp_X]/29.5mL ARSENIC TRIOXIDE - 8 [hp_X]/29.5mL BAPTISIA TINCTORIA WHOLE - 4 [hp_X]/29.5mL BRYONIA ALBA ROOT - 6 [hp_X]/29.5mL CALCIUM SULFIDE - 10 [hp_X]/29.5mL CORTISONE ACETATE - 13 [hp_X]/29.5mL ECHINACEA ANGUSTIFOLIA WHOLE - 2 [hp_X]/29.5mL EUPATORIUM PERFOLIATUM FLOWERING TOP - 6 [hp_X]/29.5mL Load more... EUPHORBIA RESINIFERA RESIN - 6 [hp_X]/29.5mL GELSEMIUM SEMPERVIRENS ROOT - 6 [hp_X]/29.5mL HAEMOPHILUS INFLUENZAE - 12 [hp_X]/29.5mL LACHESIS MUTA VENOM - 10 [hp_X]/29.5mL MERCURIC CHLORIDE - 12 [hp_X]/29.5mL PHOSPHORUS - 8 [hp_X]/29.5mL PHYTOLACCA AMERICANA ROOT - 6 [hp_X]/29.5mL PULSATILLA MONTANA WHOLE - 8 [hp_X]/29.5mL RANCID BEEF - 199 [hp_X]/29.5mL SANGUINARIA CANADENSIS ROOT - 4 [hp_X]/29.5mL SILVER NITRATE - 8 [hp_X]/29.5mL STAPHYLOCOCCUS AUREUS - 18 [hp_X]/29.5mL STREPTOCOCCUS PYOGENES - 18 [hp_X]/29.5mL SULFUR - 8 [hp_X]/29.5mL THUJA OCCIDENTALIS LEAF - 8 [hp_X]/29.5mL TOXICODENDRON PUBESCENS LEAF - 6 [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:	18 Jun, 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:	U0NQ8555JD ZY0NX0W00D O80TY208ZW S7V92P67HO 5K1UO2888Y T7J046YI2B 1MBW07J51Q 883WKN7W8X VB06AV5US8 1W0775VX6E Load more... 1TI1O9028K 639KR60Q1Q K738E2MB3I VSW71SS07I 53GH7MZT1R 27YLU75U4W 11E6VI8VEG 24K790T39B 29SUH5R3HU N9288CD508 95IT3W8JZE O478WX4004 LJ2LP0YL98 70FD1KFU70 0T0DQN8786 6IO182RP7A 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.
Pharmacologic Class:	Corticosteroid Hormone Receptor Agonists [MoA] Corticosteroid [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
63083-9222-1	29.5 mL in 1 BOTTLE, DROPPER (63083-9222-1)	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

Echinacea Combination 9222

Echinacea Combination

Liquid
Professional Complementary Health Formulas
NDC: 63083-9222

Purpose:

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

Product Elements:

Echinacea combination 9222 echinacea combination echinacea angustifolia whole echinacea angustifolia whole aconitum napellus whole aconitum napellus whole arnica montana whole arnica montana whole baptisia tinctoria whole baptisia tinctoria whole sanguinaria canadensis root sanguinaria canadensis root bryonia alba root bryonia alba root eupatorium perfoliatum flowering top eupatorium perfoliatum flowering top euphorbia resinifera resin euphorbia resinifera resin gelsemium sempervirens root gelsemium sempervirens root phytolacca americana root phytolacca americana root toxicodendron pubescens leaf toxicodendron pubescens leaf silver nitrate silver cation arsenic trioxide arsenic cation (3+) phosphorus phosphorus pulsatilla montana whole pulsatilla montana whole sulfur sulfur thuja occidentalis leaf thuja occidentalis leaf calcium sulfide calcium sulfide lachesis muta venom lachesis muta venom zinc zinc aristolochia clematitis root aristolochia clematitis root haemophilus influenzae haemophilus influenzae mercuric chloride mercuric cation cortisone acetate cortisone staphylococcus aureus staphylococcus aureus streptococcus pyogenes streptococcus pyogenes rancid beef rancid beef alcohol water

Indications and Usage:

Indications for the temporary relief of cold- and flu-like symptoms such as chills, muscle aches, cough, congestion, runny nose, occasional headache, or fatigue.*

Warnings:

Warnings persistent symptoms may be a sign of a serious condition. if symptoms persist or are accompanied by a fever, rash, or persistent headache, consult a doctor. keep out of the reach of children. in case of overdose, get medical help or contact a poison control center right away. if pregnant or breastfeeding, ask a healthcare professional before use. 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 echinacea 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.