Thymus Formula

Betula Pendula Folia Bos Taurus Thymus, Castanea Vesca, Poplar Bud, Rna

Apex Energetics Inc.
Human Otc Drug
NDC 63479-2504

Thymus Formula also known as Betula Pendula Folia Bos Taurus Thymus, Castanea Vesca, Poplar Bud, Rna is a human otc drug labeled by 'Apex Energetics Inc.'. National Drug Code (NDC) number for Thymus Formula is 63479-2504. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in Thymus Formula drug includes Betula Pendula Leaf - 2 [hp_X]/mL Bos Taurus Thymus - 7 [hp_C]/mL Castanea Sativa Leaf - 2 [hp_X]/mL Populus Balsamifera Leaf Bud - 2 [hp_X]/mL Saccharomyces Cerevisiae Rna - 4 [hp_X]/mL . The currest status of Thymus Formula drug is Active.

Drug Information:

Drug NDC:	63479-2504
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:	Thymus Formula
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:	Betula Pendula Folia Bos Taurus Thymus, Castanea Vesca, Poplar Bud, Rna
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Apex Energetics Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Solution/ Drops
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:	BETULA PENDULA LEAF - 2 [hp_X]/mL BOS TAURUS THYMUS - 7 [hp_C]/mL CASTANEA SATIVA LEAF - 2 [hp_X]/mL POPULUS BALSAMIFERA LEAF BUD - 2 [hp_X]/mL SACCHAROMYCES CEREVISIAE RNA - 4 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	SUBLINGUAL
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 Jul, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	20 Dec, 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:	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:	Apex Energetics 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:	5HW39H9KDH 8XEJ88V2T8 IV3S2HH53G 9CQ6C00G3C J17GBZ5VGX
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
63479-2504-1	30 mL in 1 BOTTLE, GLASS (63479-2504-1)	25 Jul, 2022	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.

Other medicines with the same generic name

Thymus Formula

Betula Pendula Folia Bos Taurus Thymus, Castanea Vesca, Poplar Bud, Rna

Solution/ Drops
Apex Energetics Inc.
NDC: 63479-2504

Purpose:

Uses: for temporary relief of minor: cough* fatigue* sore throat* headache* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Thymus formula betula pendula folia bos taurus thymus, castanea vesca, poplar bud, rna water populus balsamifera leaf bud populus balsamifera leaf bud saccharomyces cerevisiae rna saccharomyces cerevisiae rna betula pendula leaf betula pendula leaf bos taurus thymus bos taurus thymus castanea sativa leaf castanea sativa leaf alcohol

Indications and Usage:

Uses: for temporary relief of minor: cough* fatigue* sore throat* headache* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: if pregnant or breastfeeding , ask a health professional before use. do not use if clear seal over the cap is broken or missing. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. stop use and ask a doctor if cough, fatigue, headache, or other symptoms do not improve within 7 days or are accompanied by fever. sore throat warning : severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. consult a doctor promptly. do not use more than 2 days unless directed by a doctor.

Dosage and Administration:

Directions: adults & children ages 12 years and over: take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional. consult a physician for use in children under 12 years of age.

Stop Use:

Stop use and ask a doctor if cough, fatigue, headache, or other symptoms do not improve within 7 days or are accompanied by fever. sore throat warning : severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. consult a doctor promptly. do not use more than 2 days unless directed by a doctor.

Package Label Principal Display Panel:

The younger youÂ® dr. galitzerâs thymus formula cough* fatigue* minor sore throat* homeopathic formula 1 fl oz (30 ml) alcohol 20% by volume yy04-220614

Further Questions:

Distributed by apex energetics. questions? 16592 hale ave., irvine, ca 92606, usa

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.