Liquid Serotonin
Serotonin
Pain And Stress Center Products
Human Otc Drug
NDC 60564-0001Liquid Serotonin also known as Serotonin is a human otc drug labeled by 'Pain And Stress Center Products'. National Drug Code (NDC) number for Liquid Serotonin is 60564-0001. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Liquid Serotonin drug includes Serotonin Hydrochloride - 3 [hp_X]/mL . The currest status of Liquid Serotonin drug is Active.
Drug Information:
| Drug NDC: | 60564-0001 |
| 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: | Liquid Serotonin |
| 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: | Serotonin |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Pain And Stress Center Products |
| 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: | SEROTONIN HYDROCHLORIDE - 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: | 14 Mar, 2014 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 09 May, 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: | Pain and Stress Center Products
|
| 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: | 0648046700029
|
| UPC stands for Universal Product Code. |
| UNII: | GKN429M9VS
|
| 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 |
|---|
| 60564-0001-1 | 30 mL in 1 BOTTLE, DROPPER (60564-0001-1) | 14 Mar, 2014 | 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. |
Purpose:
Uses: temporarily eases low serotonin symptoms such as - stress-anxiety - depression - overactivity - sleeplessness serotonin is a neurotransmitter that keeps us calm, relaxed, and in control. serotonin is found in the brain and throughout the body. use liquid serotonin in conjunction with amino acids to boost serotonin.
Product Elements:
Liquid serotonin serotonin serotonin hydrochloride serotonin citric acid monohydrate water glycerin sodium benzoate
Indications and Usage:
Uses: temporarily eases low serotonin symptoms such as - stress-anxiety - depression - overactivity - sleeplessness serotonin is a neurotransmitter that keeps us calm, relaxed, and in control. serotonin is found in the brain and throughout the body. use liquid serotonin in conjunction with amino acids to boost serotonin.
Warnings:
Warnings: do not use with ssris, ssnis, maos, or tca (tricyclic anti-depressants). if pregnant or lactating, consult your health care professional before use. keep out of the reach of children. do not expose to heat. store tightly closed in a cool, dry place. safety sealed for your protection and product freshness. do not use if safety seal is broken or missing. in case of overdose, get medical help or contact a posion control center right away.
Dosage and Administration:
Directions: adults: take 15 drops under the tounge as needed up to six times a day or as directed by a health care professional. children: take 5 drops per pounds of body weight or as directed by a health care professional.
Package Label Principal Display Panel:
Package label display psc products ndc 60564-0001-1 liquid serotonin homeopathic 1 fl. oz. (30 ml) liquid serotonin
Further Questions:
Questions: distributed by pain and stress center products helotes, tx 78023 1-800-669-2256 www.painstresscenter.com