Anger

Aconitum Napellus, Asafoetida, Chamomilla, Crocus Sativus, Hyoscyamus Niger, Ignatia Amara, Sumbul, Valeriana Officinalis

Liddell Laboratories
Human Otc Drug
NDC 50845-0043

Anger also known as Aconitum Napellus, Asafoetida, Chamomilla, Crocus Sativus, Hyoscyamus Niger, Ignatia Amara, Sumbul, Valeriana Officinalis is a human otc drug labeled by 'Liddell Laboratories'. National Drug Code (NDC) number for Anger is 50845-0043. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Anger drug includes Aconitum Napellus - 200 [hp_C]/mL Asafetida - 4 [hp_X]/mL Ferula Sumbul Root - 3 [hp_X]/mL Hyoscyamus Niger - 200 [hp_C]/mL Matricaria Recutita - 3 [hp_X]/mL Saffron - 3 [hp_X]/mL Strychnos Ignatii Seed - 4 [hp_X]/mL Valerian - 3 [hp_X]/mL . The currest status of Anger drug is Active.

Drug Information:

Drug NDC:	50845-0043
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:	Anger
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:	Aconitum Napellus, Asafoetida, Chamomilla, Crocus Sativus, Hyoscyamus Niger, Ignatia Amara, Sumbul, Valeriana Officinalis
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Liddell Laboratories
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:	ACONITUM NAPELLUS - 200 [hp_C]/mL ASAFETIDA - 4 [hp_X]/mL FERULA SUMBUL ROOT - 3 [hp_X]/mL HYOSCYAMUS NIGER - 200 [hp_C]/mL MATRICARIA RECUTITA - 3 [hp_X]/mL SAFFRON - 3 [hp_X]/mL STRYCHNOS IGNATII SEED - 4 [hp_X]/mL VALERIAN - 3 [hp_X]/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:	25 Aug, 2010
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	21 Mar, 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:	07 May, 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
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 W9FZA51AS1 GLA4808EHQ 4WRK2153H3 G0R4UBI2ZZ E849G4X5YJ 1NM3M2487K JWF5YAW3QW
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
50845-0043-2	1 BOTTLE, SPRAY in 1 CARTON (50845-0043-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0043-1)	26 May, 2016	21 Mar, 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

Anger

Aconitum Napellus & more..

Spray
Liddell Laboratories
NDC: 50845-0043

Purpose:

Uses: may temporarily relieve symptoms of anger, such as: explosive outbursts feelings of hostility restlessness irritability** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Anger aconitum napellus, asafoetida, chamomilla, crocus sativus, hyoscyamus niger, ignatia amara, sumbul, valeriana officinalis aconitum napellus aconitum napellus asafetida asafetida matricaria recutita matricaria recutita saffron saffron hyoscyamus niger hyoscyamus niger strychnos ignatii seed strychnos ignatii seed ferula sumbul root ferula sumbul root valerian valerian water alcohol

Indications and Usage:

Uses: may temporarily relieve symptoms of anger, such as: explosive outbursts feelings of hostility restlessness irritability **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

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 product. do not use if tamper evident seal around neck of bottle is missing or broken. other information: store at room temperature.

Dosage and Administration:

Directions: adults and children over 12: spray twice under the tongue three times per day. for acute symptoms, dosage may be administered up to six times per 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 letting go 53 ang anger may relieve feelings of anger, such as explosive outbursts, hostility, restlessness, irritability. homeopathic doctor formulated ...when flower essences just aren't enough. 1.0 fl. oz. (30 ml) anger lbl anger 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.