Jointiva Cream
FDA Label NDC 57237-355

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Rising Pharma Holdings, Inc. for the product Jointiva (NDC 57237-355). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug factsactive ingredient, purpose, warnings, directions, other information, inactive ingredients, questions or comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Factsactive Ingredient

Trolamine Salicylate 10%                                                     

Purpose

Topical analgesic

Warnings

For external use only.

Directions

adults and children over 12 years:

  • apply generously to affected area
  • massage into painful area until thoroughly absorbed into skin
  • repeat as necessary, but no more than 4 times daily

    • children 12 years and younger: ask a doctor

Other Information

  • Store at 20° to 25°C (68° to 77°F)

Inactive Ingredients

Cetyl alcohol, disodium edetate, glycerin, light mineral oil, methyl paraben, monobasic potassium phosphate, propyl paraben, stearic acid, triethanolamine, water.

Questions Or Comments?

Call 1-844-474-7464

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