Jakemans Throat And Chest Peppermint
Menthol
Jakemans (confectioners) Ltd.
Human Otc Drug
NDC 42637-824Jakemans Throat And Chest Peppermint also known as Menthol is a human otc drug labeled by 'Jakemans (confectioners) Ltd.'. National Drug Code (NDC) number for Jakemans Throat And Chest Peppermint is 42637-824. This drug is available in dosage form of Lozenge. The names of the active, medicinal ingredients in Jakemans Throat And Chest Peppermint drug includes Menthol - 5 mg/1 . The currest status of Jakemans Throat And Chest Peppermint drug is Active.
Drug Information:
| Drug NDC: | 42637-824 |
| 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: | Jakemans Throat And Chest Peppermint |
| 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: | Menthol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Jakemans (confectioners) Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Lozenge |
| 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: | MENTHOL - 5 mg/1
|
| 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: | OTC MONOGRAPH FINAL |
| 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 Dec, 2013 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 05 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. |
| Application Number: | part341 |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| 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: | Jakemans (Confectioners) Ltd.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 311508
2046635
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0811721020013
|
| UPC stands for Universal Product Code. |
| UNII: | L7T10EIP3A
|
| 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 |
|---|
| 42637-824-01 | 30 LOZENGE in 1 PACKAGE (42637-824-01) | 11 Dec, 2013 | N/A | No |
| 42637-824-02 | 24 LOZENGE in 1 PACKAGE (42637-824-02) | 11 Dec, 2013 | 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:
Jakemans® boston england est 1907 throat & chest⢠peppermint flavored menthol cough suppressant oral anesthetic made in boston, england, for over 100 years using the finest natural ingredients. 30 lozenges jakemans famous and original throat & chest lozenges are made with the finest natural ingredients, carefully blended with soothing menthol to obtain a unique mouth watering and refreshing taste. once tasted they will be your favorite soothing lozenge! manufactured by: jakemans (confectioners) ltd. boston pe20 2ja, united kingdom us toll free: 1-866-205-1185 www.jakemans.us
Product Elements:
Jakemans throat and chest peppermint menthol corn syrup sucrose water peppermint oil menthol menthol ol
Indications and Usage:
Uses temporarily relieves cough due to minor throat and bronchial irritation occurring with the common cold or inhaled irritants. occasional minor irritation, pain, sore mouth, and sore throat.
Warnings:
Warnings sore throat warning if sore throat is severe, persists more than 2 days, is accompanied or followed by fever ,headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. ask a doctor before use if you have persistent or chronic cough as occurs with smoking, asthma or emphysema cough that occurs with excessive phlegm (mucus). stop use and ask a doctor if cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. a persistent cough may be a sign of a serious condition. sore mouth symptoms do not improve in 7 days. if pregnant or breast-feeding, ask a health professional before use.
Dosage and Administration:
Directions adults and children 2 years and over: dissolve lozenge slowly in the mouth. repeat every 2 hours as needed or as directed by a doctor. children under 2 years of age: ask a doctor.
Package Label Principal Display Panel:
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