Telomere - Dna

Ca98, Carotenoid, Dna, Glutathione, Omega 3, Pituitarum, Rna, Vitamin B Complex, Vitamin C, Vitamin D3, Vitamin E

Problen
Human Otc Drug
NDC 43853-0027

Telomere - Dna also known as Ca98, Carotenoid, Dna, Glutathione, Omega 3, Pituitarum, Rna, Vitamin B Complex, Vitamin C, Vitamin D3, Vitamin E is a human otc drug labeled by 'Problen'. National Drug Code (NDC) number for Telomere - Dna is 43853-0027. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Telomere - Dna drug includes .alpha.-tocopherol - 12 [hp_X]/30mL Ascorbic Acid - 12 [hp_X]/30mL Beta Carotene - 12 [hp_X]/30mL Cholecalciferol - 12 [hp_X]/30mL Cyanocobalamin - 12 [hp_X]/30mL Cycloastragenol - 12 [hp_X]/30mL Glutathione - 12 [hp_X]/30mL Herring Sperm Dna - 9 [hp_X]/30mL Omega-3 Fatty Acids - 12 [hp_X]/30mL Pantothenic Acid - 12 [hp_X]/30mL and more. The currest status of Telomere - Dna drug is Active.

Drug Information:

Drug NDC:	43853-0027
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:	Telomere - Dna
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:	Ca98, Carotenoid, Dna, Glutathione, Omega 3, Pituitarum, Rna, Vitamin B Complex, Vitamin C, Vitamin D3, Vitamin E
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Problen
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:	.ALPHA.-TOCOPHEROL - 12 [hp_X]/30mL ASCORBIC ACID - 12 [hp_X]/30mL BETA CAROTENE - 12 [hp_X]/30mL CHOLECALCIFEROL - 12 [hp_X]/30mL CYANOCOBALAMIN - 12 [hp_X]/30mL CYCLOASTRAGENOL - 12 [hp_X]/30mL GLUTATHIONE - 12 [hp_X]/30mL HERRING SPERM DNA - 9 [hp_X]/30mL OMEGA-3 FATTY ACIDS - 12 [hp_X]/30mL PANTOTHENIC ACID - 12 [hp_X]/30mL Load more... RIBOFLAVIN - 12 [hp_X]/30mL SACCHAROMYCES CEREVISIAE RNA - 9 [hp_X]/30mL SUS SCROFA PITUITARY GLAND, POSTERIOR - 5 [hp_C]/30mL THIAMINE - 12 [hp_X]/30mL
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:	01 Nov, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	24 Jun, 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:	ProBLEN
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.
NUI:	N0000193618 M0001797 M0022797 N0000175952 M0022794 N0000175951 M0023885 N0000175583
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	H4N855PNZ1 PQ6CK8PD0R 01YAE03M7J 1C6V77QF41 P6YC3EG204 X37D9F2L0V GAN16C9B8O 51FI676N6F 71M78END5S 19F5HK2737 Load more... TLM2976OFR J17GBZ5VGX E8S87O660T X66NSO3N35
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 EPC:	Vitamin C [EPC] Vitamin D [EPC] Vitamin B12 [EPC] Omega-3 Fatty Acid [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:	Ascorbic Acid [CS] Vitamin D [CS] Vitamin B 12 [CS] Fatty Acids, Omega-3 [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Ascorbic Acid [CS] Fatty Acids Omega-3 [CS] Omega-3 Fatty Acid [EPC] Vitamin B 12 [CS] Vitamin B12 [EPC] Vitamin C [EPC] Vitamin D [CS] Vitamin D [EPC]
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
43853-0027-1	30 mL in 1 BOTTLE, SPRAY (43853-0027-1)	01 Nov, 2019	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

Telomere - Dna

Ca98 & more..

Spray
ProBLEN
NDC: 43853-0027

Purpose:

Ndc: 43853-0027-1 telomere / dna homeopathic organotherapy 1 oz. bottle label temporarily supports the body's ability to maintain or rebuild telomere length, aid cellular function, and gaurd against dna damage.*

Temporarily supports the body's ability to maintain or rebuild telomere length, aid cellular function, and gaurd against dna damage.*

Product Elements:

Telomere - dna ca98, carotenoid, dna, glutathione, omega 3, pituitarum, rna, vitamin b complex, vitamin c, vitamin d3, vitamin e alcohol water cycloastragenol cycloastragenol beta carotene .beta.-carotene herring sperm dna herring sperm dna glutathione glutathione omega-3 fatty acids omega-3 fatty acids sus scrofa pituitary gland, posterior sus scrofa pituitary gland, posterior saccharomyces cerevisiae rna saccharomyces cerevisiae rna thiamine thiamine ion riboflavin riboflavin pantothenic acid pantothenic acid cyanocobalamin cyanocobalamin ascorbic acid ascorbic acid cholecalciferol cholecalciferol .alpha.-tocopherol .alpha.-tocopherol

Indications and Usage:

Uses: temporarily supports the body's ability to maintain or rebuild telomere length, aid cellular function and guard against dna damage.*

Warnings:

Warnings: not for use on children. if symptoms continue to recur, or if sleeplessness persists continuously for more than two weeks, consult a physician. i nsomnia may be a symptom of a serious underlying medical illness. as with all medicines, if you are pregnant or breast feeding, consult a health professional before using this product. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. keep out of reach of children.

Dosage and Administration:

Directions: adults: hold the spray-top close to your open mouth and spray twice directly under your tongue, three times a day. some people notice improvement within three weeks, others take longer.

Package Label Principal Display Panel:

Further Questions:

Distributed by: problen (888) 326-2121 3021 ridge rd., rockwall, tx 75032

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.