Natural Pain Relief Foot Cream
Camphor
Neat Feat Products Limited
Human Otc Drug
NDC 50017-033Natural Pain Relief Foot Cream also known as Camphor is a human otc drug labeled by 'Neat Feat Products Limited'. National Drug Code (NDC) number for Natural Pain Relief Foot Cream is 50017-033. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Natural Pain Relief Foot Cream drug includes Camphor (natural) - 1.5 g/50g . The currest status of Natural Pain Relief Foot Cream drug is Active.
Drug Information:
| Drug NDC: | 50017-033 |
| 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: | Natural Pain Relief Foot Cream |
| 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: | Camphor |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Neat Feat Products Limited |
| 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: | CAMPHOR (NATURAL) - 1.5 g/50g
|
| 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: | 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: | 19 Jan, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 17 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, 2024 |
| 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: | Neat Feat Products Limited
|
| 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: | N20HL7Q941
|
| 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 |
|---|
| 50017-033-02 | 1 TUBE in 1 BOX (50017-033-02) / 50 g in 1 TUBE (50017-033-01) | 19 Jan, 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. |
Purpose:
For the temporary relief of pain
Product Elements:
Natural pain relief foot cream camphor peg-6 sorbitan oleate glycerin rosemary oil eucalyptus oil potassium sorbate decyl glucoside frankincense oil clove oil camphor (natural) camphor (natural) anhydrous citric acid peppermint oil water arnica montana cajuput oil
Indications and Usage:
For the temporary relief of pain.
Warnings:
For external use only. avoid con1act with eyes. if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. do not use on broken or irritated skin. slop use and ask a doctor if skin irritation develops. if pregnant or tnnt feeding, ask a health professional before use. keep out of reach of chlklren, in case of overdose, get medical help or contact a poison control center right away.
Dosage and Administration:
Adults and chlldren 2 years of age and older: apply to affected area not more than 3 to 4 times daily. children under 2 years of age: consult a doclor.
Package Label Principal Display Panel:
50 g ndc: 82309-033-01 label 50 g camphor 3% .................... natural pain relieving cream for the temporary relief of pain for external use only. avoid con1act with eyes. if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. do not use on broken or irritated skin. slop use and ask a doctor if skin irritation develops. if pregnant or tnnt feeding, ask a health professional before use. keep out of reach of chlklren, in case of overdose, get medical help or contact a poison control center right away. for the temporary relief of pain. keep out of reach of childen, in case of overdose, get medical help or contact a poison control center right away. adults and chlldren 2 years of age and older: apply to affected area not more than 3 to 4 times daily. children under 2 years of age: consult a doclor. shake well prior to use. store below 30c/86f decyl polyglucoside, water, sorbitan oleate, glycerin, peppermint oil, rosemary oil, frankincense oil, amica montana extract, cajeput oil, eucalyptus oil, clove bud oil, potassium sorbate, anhydrous citric acid.