Mega Patch
FDA Label NDC 82219-411

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Greenhill Trading, Inc. for the product Mega Patch (NDC 82219-411). 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 facts active ingredients, purpose, warnings:, otc - keep out of reach of children, warnings and precautions, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts Active Ingredients

Capsaicin 0.0375%

Lidocaine 4%

Menthol 5%

Methyl Salicylate 20%

Purpose

Topical Analgesic

Warnings:

For external use only.

  • Use only as directed.
  • Avoid contact with eyes and mucous membranes.
  • Do not use with heating devices or pads.
  • Do not use on wounds, cuts, damaged or infected skin as well as in the eyes, mouth, genitals, or any other mucous membranes.
  • Do not cover with bandages.

Otc - Keep Out Of Reach Of Children

Keep out of reach of chlidren.

If swallowed, call poison control.

If contact does occur with eyes, rinse with cold water and call a doctor.

Warnings And Precautions

Children under 12 years old, consult a doctor before use.

  • If you are allergic to any ingredients in this product consult a doctor before use.
  • Consult your physician: If pregnant or if pain persists or worsens.

Principal Display Panel

NDC: 82219-411-10

GREENHILL
TRADING
INC

Mega Patch

With Capsaicin 0.0375%, Lidocaine 4%,
Menthol 5%, Methyl Salicylate 20%

10 PATCHES
Patch size 10x14 CM

EXTENDED
RELEASE

Figure (Megapatch)

Figure (Megapatch)

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