Clear My Throat

Taraxacum Officinale, Sarsaparilla (smilax Regelii), Kali Phosphoricum, Natrum Muriaticum, Coffea Cruda, Glandula Suprarenalis Suis, Adenosinum Cyclophosphoricum, Silicea, Hypothalamus Suis, Thyroidinum (bovine)

Shirley Dieu Dba Clear My Throat
Human Otc Drug
NDC 78892-0001

Clear My Throat also known as Taraxacum Officinale, Sarsaparilla (smilax Regelii), Kali Phosphoricum, Natrum Muriaticum, Coffea Cruda, Glandula Suprarenalis Suis, Adenosinum Cyclophosphoricum, Silicea, Hypothalamus Suis, Thyroidinum (bovine) is a human otc drug labeled by 'Shirley Dieu Dba Clear My Throat'. National Drug Code (NDC) number for Clear My Throat is 78892-0001. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Clear My Throat drug includes Adenosine Cyclic Phosphate - 12 [hp_X]/mL Arabica Coffee Bean - 9 [hp_X]/mL Dibasic Potassium Phosphate - 6 [hp_X]/mL Silicon Dioxide - 12 [hp_X]/mL Smilax Ornata Root - 4 [hp_X]/mL Sodium Chloride - 8 [hp_X]/mL Sus Scrofa Adrenal Gland - 9 [hp_X]/mL Sus Scrofa Hypothalamus - 12 [hp_X]/mL Taraxacum Officinale - 4 [hp_X]/mL Thyroid, Bovine - 12 [hp_X]/mL . The currest status of Clear My Throat drug is Active.

Drug Information:

Drug NDC:	78892-0001
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:	Clear My Throat
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:	Taraxacum Officinale, Sarsaparilla (smilax Regelii), Kali Phosphoricum, Natrum Muriaticum, Coffea Cruda, Glandula Suprarenalis Suis, Adenosinum Cyclophosphoricum, Silicea, Hypothalamus Suis, Thyroidinum (bovine)
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Shirley Dieu Dba Clear My Throat
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:	ADENOSINE CYCLIC PHOSPHATE - 12 [hp_X]/mL ARABICA COFFEE BEAN - 9 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE - 6 [hp_X]/mL SILICON DIOXIDE - 12 [hp_X]/mL SMILAX ORNATA ROOT - 4 [hp_X]/mL SODIUM CHLORIDE - 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 9 [hp_X]/mL SUS SCROFA HYPOTHALAMUS - 12 [hp_X]/mL TARAXACUM OFFICINALE - 4 [hp_X]/mL THYROID, BOVINE - 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:	04 Aug, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	06 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:	Shirley Dieu dba Clear My Throat
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:	N0000185371 N0000185375 N0000175629 N0000184306 M0000728 M0006342 M0016962 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	E0399OZS9N 3SW678MX72 CI71S98N1Z ETJ7Z6XBU4 2H1576D5WG 451W47IQ8X 398IYQ16YV N6R0856Z79 39981FM375 MN18OTN73W
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:	Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [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 PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Plant Proteins [CS] Seed Storage Proteins [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:	Allergens [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Plant Proteins [CS] Seed Storage Proteins [CS]
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
78892-0001-1	60 mL in 1 BOTTLE, DROPPER (78892-0001-1)	04 Aug, 2020	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

Clear My Throat

Taraxacum Officinale & more..

Liquid
Shirley Dieu dba Clear My Throat
NDC: 78892-0001

Purpose:

Indications: helps to hydrate throat in an aid to reduce food obstruction when used daily.

Product Elements:

Clear my throat taraxacum officinale, sarsaparilla (smilax regelii), kali phosphoricum, natrum muriaticum, coffea cruda, glandula suprarenalis suis, adenosinum cyclophosphoricum, silicea, hypothalamus suis, thyroidinum (bovine) taraxacum officinale taraxacum officinale smilax ornata root sarsaparilla dibasic potassium phosphate phosphate ion sodium chloride chloride ion arabica coffee bean arabica coffee bean sus scrofa adrenal gland sus scrofa adrenal gland adenosine cyclic phosphate adenosine cyclic phosphate silicon dioxide silicon dioxide sus scrofa hypothalamus sus scrofa hypothalamus thyroid, bovine thyroid, bovine water glycerin alcohol

Indications and Usage:

Indications: helps to hydrate throat in an aid to reduce food obstruction when used daily.

Warnings:

Warnings: if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. do not use if tamper evident seal is broken or missing. store in a cool, dry place.

Dosage and Administration:

Directions: shake bottle before use. twice a day, add 8 drips to 16 oz. of liquid and stir. must be added to liquid such as water, coffee, tea, soup, etc. measure according. 4 drops per cup to total 16 drops per day. daily usage is recommended to obtain clear my throat's full effect. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: clear my throat helps reduce food obstruction homeopathic 2 fl. oz. (60 ml) clear my throat

Further Questions:

Questions: dist. by: clear my throat irvine, ca 92618 949-387-9090

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.