Dosage & Administration
Apply one patch up to 3 times per day. Do not leave on skin for more than a total of 8 hours per day • Repeat as necessary, but no more than 3 times daily.
Topcare Pain Relief Patch
FDA Label NDC 76162-999
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by 76162 for the product Topcare Pain Relief Patch (NDC 76162-999). 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 dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
Warnings:
For external use only
Inactive Ingredient
Inactive ingredients
Dihydroxyaluminum aminoacetate, DMDM Hydantoin, Edetic acid, Glycerin, Isopropyl myristate, Polyacrylic acid, Polysorbate 80,
Polyvinyl alcohol, Propylene glycol, Sodium polyacrylate, Tartaric acid, Titanium dioxide, Water.
Indications & Usage
Purpose: Topical analgesic
Uses: Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises,
sprains.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Purpose
Purpose:
Topical analgesic
Package Label.Principal Display Panel
Drug facts, Active ingredients, Purpose, Uses, Warnings, Do not use, When using this product, Stop use and asks a doctor if, If pregnant or breast, Keep out of children, Directions, Other information, Inactive ingredients
* Please review the disclaimer below.
