Trimotion Pain Relief
Menthol, Methyl Salicylate
Naturemed, Inc
Human Otc Drug
NDC 45632-736Trimotion Pain Relief also known as Menthol, Methyl Salicylate is a human otc drug labeled by 'Naturemed, Inc'. National Drug Code (NDC) number for Trimotion Pain Relief is 45632-736. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Trimotion Pain Relief drug includes Menthol - 25 mg/g Methyl Salicylate - 100 mg/g . The currest status of Trimotion Pain Relief drug is Active.
Drug Information:
| Drug NDC: | 45632-736 |
| 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: | Trimotion Pain Relief |
| 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, Methyl Salicylate |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Naturemed, Inc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Cream |
| 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 - 25 mg/g
METHYL SALICYLATE - 100 mg/g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| 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 NOT 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: | 06 Apr, 2016 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 15 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: | part348 |
| 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: | NatureMed, Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1148131
|
| 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. |
| UNII: | L7T10EIP3A
LAV5U5022Y
|
| 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 |
|---|
| 45632-736-01 | 1 BOTTLE, PLASTIC in 1 BOX (45632-736-01) / 57 g in 1 BOTTLE, PLASTIC | 06 Apr, 2016 | 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:
Purpose topical analgesic
Product Elements:
Trimotion pain relief menthol, methyl salicylate cucumber dimethyl sulfone emu oil gluconolactone glucosamine sulfate glycerin sunflower oil tea tree oil propanediol salix alba bark sodium benzoate sorbitan olivate xanthan gum menthol menthol methyl salicylate salicylic acid aloe vera leaf chamaemelum nobile flower water arnica montana indian frankincense calendula officinalis flower cetearyl olivate
Indications and Usage:
Uses: for the temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.
Warnings:
Warnings: for external use only. when using this product use only as directed do not bandage tightly or use with aheating pad do not apply to wounds or damaged skin avoid contact with eyes or mucous membranes. stop use and ask a doctor if condition worsens irritation develops redness is present symptoms persist for more than 7 days or clear up and occur again within a few days if pregnant or breastfeeding ask a health professional prior to use. keep out of reach of children. if swallowed, get medical help or contact poison control immediately.
When Using:
When using this product use only as directed do not bandage tightly or use with aheating pad do not apply to wounds or damaged skin avoid contact with eyes or mucous membranes.
Dosage and Administration:
Directions: adults and children 12 years of age or older: apply to affected area not more than three to four times daily. children under 12 years of age: consult a physician.
Stop Use:
Stop use and ask a doctor if condition worsens irritation develops redness is present symptoms persist for more than 7 days or clear up and occur again within a few days
Package Label Principal Display Panel:
Package labeling: label
Further Questions:
Questions or comments? call 1-800-218-1379