Coralite Ultra Strength Pain Relief
Camphor Menthol
United Exchange Corp.
Human Otc Drug
NDC 65923-532Coralite Ultra Strength Pain Relief also known as Camphor Menthol is a human otc drug labeled by 'United Exchange Corp.'. National Drug Code (NDC) number for Coralite Ultra Strength Pain Relief is 65923-532. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Coralite Ultra Strength Pain Relief drug includes Camphor (synthetic) - 110 mg/g Menthol - 110 mg/g . The currest status of Coralite Ultra Strength Pain Relief drug is Active.
Drug Information:
| Drug NDC: | 65923-532 |
| 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: | Coralite Ultra Strength 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: | Camphor Menthol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | United Exchange Corp. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Ointment |
| 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 (SYNTHETIC) - 110 mg/g
MENTHOL - 110 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: | 15 Oct, 2014 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 16 Jan, 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. |
| 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: | United Exchange Corp.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1089831
|
| 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: | 5TJD82A1ET
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 |
|---|
| 65923-532-18 | 1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR | 13 Dec, 2017 | 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:
Uses temporarily relieves minor aches and pains of muscles and joints associated with simple backache arthritis strains bruise sprains
Product Elements:
Coralite ultra strength pain relief camphor menthol peppermint oil peppermint clove oil petrolatum paraffin camphor (synthetic) camphor (synthetic) menthol menthol
Indications and Usage:
Directions adults and children 12 years of age and older: rub well on the affected area. repeat 3 to 4 times daily. children under 12 years of age: consult a doctor
Warnings:
Warnings for external use only allergy alert: this product may cause allergic reaction in some individuals. test on small area before use.
Do Not Use:
Warnings for external use only allergy alert: this product may cause allergic reaction in some individuals. test on small area before use.
When Using:
When using this product do not use otherwise than as directed avoid contact with the eyes, mucous membranes or rashes do not bandage tightly discontinue use at least 1 hour before a bath or shower do not use immediately after a bath or shower
Dosage and Administration:
Distributed by: united exchange corp. cypress, ca 90630 usa 1-888-645-8204 made in china
Stop Use:
Stop use and ask a doctor if redness is present or irritation or rash develops condition worsens or symptoms persist for more than 7 days symptoms clear up and occur again within a few days
Package Label Principal Display Panel:
532.1