Sinus Congestion Headache

Antimonium Tartaricum, Arsenicum Iodatum, Asafoetida, Baptisia Tinctoria, Echinacea (angustifolia), Eupatorium Perfoliatum, Euphorbia Pilulifera, Hepar Sulphuris Calcareum, Hydrastis Canadensis, Kali Bichromicum, Kreosotum, Lachesis Mutus, Magnesia Carbonica, Pyrogenium, Silicea, Teucrium Marum

Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0243

Sinus Congestion Headache also known as Antimonium Tartaricum, Arsenicum Iodatum, Asafoetida, Baptisia Tinctoria, Echinacea (angustifolia), Eupatorium Perfoliatum, Euphorbia Pilulifera, Hepar Sulphuris Calcareum, Hydrastis Canadensis, Kali Bichromicum, Kreosotum, Lachesis Mutus, Magnesia Carbonica, Pyrogenium, Silicea, Teucrium Marum is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Sinus Congestion Headache is 50845-0243. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Sinus Congestion Headache drug includes Antimony Potassium Tartrate - 6 [hp_X]/mL Arsenic Triiodide - 200 [hp_C]/mL Asafetida - 30 [hp_C]/mL Baptisia Tinctoria Root - 3 [hp_X]/mL Calcium Sulfide - 30 [hp_X]/mL Echinacea Angustifolia - 3 [hp_X]/mL Eupatorium Perfoliatum Flowering Top - 6 [hp_X]/mL Euphorbia Hirta Flowering Top - 3 [hp_X]/mL Goldenseal - 30 [hp_C]/mL Lachesis Muta Venom - 200 [hp_X]/mL and more. The currest status of Sinus Congestion Headache drug is Active.

Drug Information:

Drug NDC:	50845-0243
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:	Sinus Congestion Headache
Also known as the trade name. It is the name of the product chosen by the labeler.
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:	Antimonium Tartaricum, Arsenicum Iodatum, Asafoetida, Baptisia Tinctoria, Echinacea (angustifolia), Eupatorium Perfoliatum, Euphorbia Pilulifera, Hepar Sulphuris Calcareum, Hydrastis Canadensis, Kali Bichromicum, Kreosotum, Lachesis Mutus, Magnesia Carbonica, Pyrogenium, Silicea, Teucrium Marum
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Liddell Laboratories, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Spray
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:	ANTIMONY POTASSIUM TARTRATE - 6 [hp_X]/mL ARSENIC TRIIODIDE - 200 [hp_C]/mL ASAFETIDA - 30 [hp_C]/mL BAPTISIA TINCTORIA ROOT - 3 [hp_X]/mL CALCIUM SULFIDE - 30 [hp_X]/mL ECHINACEA ANGUSTIFOLIA - 3 [hp_X]/mL EUPATORIUM PERFOLIATUM FLOWERING TOP - 6 [hp_X]/mL EUPHORBIA HIRTA FLOWERING TOP - 3 [hp_X]/mL GOLDENSEAL - 30 [hp_C]/mL LACHESIS MUTA VENOM - 200 [hp_X]/mL Load more... MAGNESIUM CARBONATE - 10 [hp_X]/mL POTASSIUM DICHROMATE - 30 [hp_C]/mL RANCID BEEF - 200 [hp_C]/mL SILICON DIOXIDE - 30 [hp_C]/mL TEUCRIUM MARUM - 3 [hp_X]/mL WOOD CREOSOTE - 30 [hp_C]/mL
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:	16 Oct, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	16 Oct, 2023
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:	23 Dec, 2025
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:	Liddell Laboratories, Inc.
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:	DL6OZ476V3 3029988O2T W9FZA51AS1 5EF0HWI5WU 1MBW07J51Q VB06AV5US8 1W0775VX6E 6H89ZY31MR ZW3Z11D0JV VSW71SS07I Load more... 0E53J927NA T4423S18FM 29SUH5R3HU ETJ7Z6XBU4 10464S0TAA 3JYG22FD73
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
50845-0243-1	30 mL in 1 BOTTLE, SPRAY (50845-0243-1)	16 Oct, 2018	16 Oct, 2023	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

Sinus Congestion Headache

Antimonium Tartaricum & more..

Spray
Liddell Laboratories, Inc.
NDC: 50845-0243

Purpose:

Uses: may temporarily aid in sinus drainage and temporarily relieve these symptoms associated with sinus congestion and sinus related headache: â¢ sinus congestion â¢ sinus pressure â¢ headache pain** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Sinus congestion headache antimonium tartaricum, arsenicum iodatum, asafoetida, baptisia tinctoria, echinacea (angustifolia), eupatorium perfoliatum, euphorbia pilulifera, hepar sulphuris calcareum, hydrastis canadensis, kali bichromicum, kreosotum, lachesis mutus, magnesia carbonica, pyrogenium, silicea, teucrium marum antimony potassium tartrate antimony cation (3+) arsenic triiodide arsenic cation (3+) asafetida asafetida baptisia tinctoria root baptisia tinctoria root echinacea angustifolia echinacea angustifolia eupatorium perfoliatum flowering top eupatorium perfoliatum flowering top euphorbia hirta flowering top euphorbia hirta flowering top calcium sulfide calcium sulfide goldenseal goldenseal potassium dichromate dichromate ion wood creosote wood creosote lachesis muta venom lachesis muta venom magnesium carbonate carbonate ion rancid beef rancid beef silicon dioxide silicon dioxide teucrium marum teucrium marum water alcohol

Indications and Usage:

Warnings:

Warnings: do not use if you have ever had an allergic reaction to this product or any of its ingredients. stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur. keep out of reach of children. in case of overdose, get medical help or call a poison control center right away. if pregnant or breast feeding, ask a doctor before using this product. do not use if tamper evident seal around neck of bottle is missing or broken. store at room temperature.

Dosage and Administration:

Directions: adults and children over 12: spray twice under the tongue three times per day. for severe symptoms, dosage may be taken up to six times the first day. children 12 and under: consult a doctor prior to use.

Package Label Principal Display Panel:

Package label display: oral sprays liddell laboratories est. 1994 09 sch sinus congestion + headache may aid in sinus drainage + relieve these symptoms: sinus congestion, sinus pressure + headache pain. homeopathic doctor formulated readily absorbed. safe. no known side effects. easy to use. 1.0 fl oz. (30 ml) sinus congestion + headache lbl sinus congestion + headache ctn

Further Questions:

Questions: dist. by liddell laboratories, inc. 201 apple blvd. woodbine, ia 51579 www.liddell.net 1-800-460-7733

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.