Overwhelmed

Antimonium Crudum, Arsenicum Album, Baryta Carbonica, Calcarea Phosphorica, Calcarea Silicata, Cicuta Virosa, Conium Maculatum

Liddell Laboratories
Human Otc Drug
NDC 50845-0053

Overwhelmed also known as Antimonium Crudum, Arsenicum Album, Baryta Carbonica, Calcarea Phosphorica, Calcarea Silicata, Cicuta Virosa, Conium Maculatum is a human otc drug labeled by 'Liddell Laboratories'. National Drug Code (NDC) number for Overwhelmed is 50845-0053. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Overwhelmed drug includes Antimony Trisulfide - 30 [hp_C]/mL Arsenic Trioxide - 30 [hp_C]/mL Barium Carbonate - 12 [hp_C]/mL Calcium Silicate - 12 [hp_X]/mL Cicuta Virosa Root - 30 [hp_C]/mL Conium Maculatum Flowering Top - 30 [hp_C]/mL Tribasic Calcium Phosphate - 12 [hp_X]/mL . The currest status of Overwhelmed drug is Active.

Drug Information:

Drug NDC:	50845-0053
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:	Overwhelmed
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 Crudum, Arsenicum Album, Baryta Carbonica, Calcarea Phosphorica, Calcarea Silicata, Cicuta Virosa, Conium Maculatum
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:	ANTIMONY TRISULFIDE - 30 [hp_C]/mL ARSENIC TRIOXIDE - 30 [hp_C]/mL BARIUM CARBONATE - 12 [hp_C]/mL CALCIUM SILICATE - 12 [hp_X]/mL CICUTA VIROSA ROOT - 30 [hp_C]/mL CONIUM MACULATUM FLOWERING TOP - 30 [hp_C]/mL TRIBASIC CALCIUM PHOSPHATE - 12 [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:	11 Aug, 2010
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	19 Oct, 2025
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 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:	F79059A38U S7V92P67HO 6P669D8HQ8 S4255P4G5M YEA9P21S8N Q28R5GF371 91D9GV0Z28
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:	Blood Coagulation Factor [EPC] Calcium [CS] Cations Divalent [CS] Increased Coagulation Factor Activity [PE]
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
50845-0053-2	1 BOTTLE, SPRAY in 1 CARTON (50845-0053-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0053-1)	15 Sep, 2016	19 Oct, 2025	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

Overwhelmed

Antimonium Crudum & more..

Spray
Liddell Laboratories
NDC: 50845-0053

Purpose:

Indications: may temporarily relieve symptoms of feeling overwhelmed (without the side effects of narcotic or habit forming drugs), such as: indecisiveness self-doubt mental fatigue physical fatigue** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Overwhelmed antimonium crudum, arsenicum album, baryta carbonica, calcarea phosphorica, calcarea silicata, cicuta virosa, conium maculatum antimony trisulfide antimony cation (3+) arsenic trioxide arsenic cation (3+) barium carbonate barium cation tribasic calcium phosphate phosphate ion calcium silicate calcium cation cicuta virosa root cicuta virosa root conium maculatum flowering top conium maculatum flowering top water alcohol

Indications and Usage:

Indications: may temporarily relieve symptoms of feeling overwhelmed (without the side effects of narcotic or habit forming drugs), such as: â¢ indecisiveness â¢ self-doubt â¢ mental fatigue â¢ physical fatigue** **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 up to six times per day until symptoms are relieved. 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 52 ovr overwhelmed may relieve symptoms of feeling overwhelmed such as self-doubt, indecisiveness, and uncertainty. homeopathic doctor formulated ...when flower essences just aren't enough. 1.0 fl. oz. (30 ml) overwhelmed lbl overwhelmed ctn

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.