Injuries

Anthracinum, Arnica Montana, Bellis Perennis, Calendula Officinalis, Echinacea (angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Pyrogenium

Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0183

Injuries also known as Anthracinum, Arnica Montana, Bellis Perennis, Calendula Officinalis, Echinacea (angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Pyrogenium is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Injuries is 50845-0183. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Injuries drug includes Arnica Montana - 3 [hp_X]/mL Bacillus Anthracis Immunoserum Rabbit - 30 [hp_C]/mL Bellis Perennis - 3 [hp_X]/mL Calendula Officinalis Flowering Top - 3 [hp_X]/mL Echinacea Angustifolia - 3 [hp_X]/mL Hamamelis Virginiana Root Bark/stem Bark - 3 [hp_X]/mL Hypericum Perforatum - 3 [hp_X]/mL Rancid Beef - 200 [hp_C]/mL . The currest status of Injuries drug is Active.

Drug Information:

Drug NDC:	50845-0183
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:	Injuries
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:	Anthracinum, Arnica Montana, Bellis Perennis, Calendula Officinalis, Echinacea (angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Pyrogenium
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:	ARNICA MONTANA - 3 [hp_X]/mL BACILLUS ANTHRACIS IMMUNOSERUM RABBIT - 30 [hp_C]/mL BELLIS PERENNIS - 3 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP - 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA - 3 [hp_X]/mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - 3 [hp_X]/mL HYPERICUM PERFORATUM - 3 [hp_X]/mL RANCID BEEF - 200 [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:	18 Apr, 2012
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	27 Nov, 2024
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:	09 Jun, 2026
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.
UPC:	0363113126969
UPC stands for Universal Product Code.
UNII:	O80TY208ZW 41LZ22DD4N 2HU33I03UY 18E7415PXQ VB06AV5US8 T7S323PKJS XK4IUX8MNB 29SUH5R3HU
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
50845-0183-1	30 mL in 1 BOTTLE, SPRAY (50845-0183-1)	18 Apr, 2012	27 Nov, 2024	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

Injuries

Anthracinum & more..

Spray
Liddell Laboratories, Inc.
NDC: 50845-0183

Purpose:

Indications: may temporarily relieve symptoms associated with injuries: inflammation, bruising, slow healing, pain.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Injuries anthracinum, arnica montana, bellis perennis, calendula officinalis, echinacea (angustifolia), hamamelis virginiana, hypericum perforatum, pyrogenium bacillus anthracis immunoserum rabbit bacillus anthracis immunoserum rabbit arnica montana arnica montana bellis perennis bellis perennis calendula officinalis flowering top calendula officinalis flowering top echinacea angustifolia echinacea angustifolia hamamelis virginiana root bark/stem bark hamamelis virginiana root bark/stem bark hypericum perforatum hypericum perforatum rancid beef rancid beef water alcohol

Indications and Usage:

Warnings:

Warnings: if symptoms persist for more than 7 days, consult a doctor. if pregnant or breast feeding, ask a doctor before use. keep out of reach of children. in case of overdose, get medical help or call a poison control center right away. do not use if tamper evident seal around neck of bottle is missing or broken.

Dosage and Administration:

Directions: adults and children over 12: spray twice under the tongue 3 times per day. can be sprayed topically on affected area for added relief. children 12 and under: consult a doctor prior to use.

Package Label Principal Display Panel:

Package label display: oral sprays liddell laboratories est 1994 30 inj injuries homeopathic 1.0 fl. oz. (30 ml) injuries

Further Questions:

Questions: dist. by liddell laboratories inc. 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.