Pain Relief Roll On Liquid
FDA Label NDC 79804-282

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Eagle Labs Inc for the product Pain Relief Roll On (NDC 79804-282). 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 active ingredient, purpose, uses:, warnings, when using this product, stop usage immediately and ask a doctor if:, if pregnant or breast-feeding:, keep out of reach of children:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Menthol 6%

Camphor 5%

Capsaicin 0.025%

Purpose

Topical Analgesic

Uses:

For the temporary relief of aches and pains of muscles and joints associated with arthritis, backaches, strains or sprains

Warnings

For External use only

When Using This Product

Use only as directed. Avoid contact with eyes or mucous membranes. Do not apply directly to wounds or damaged skin. Do not use in combination with other ointments, creams, or sprays. Wash hand with cool water after each uyse. Do not use with a heating pad or device. 

Stop Usage Immediately And Ask A Doctor If:

Condition worsens or symptoms persist for more than 7 days

If Pregnant Or Breast-Feeding:

Ask a health professional before use

Keep Out Of Reach Of Children:

If ingested get medical help or contact Poison control center immediately: 1-800-222-1222

Directions:

Adults and Children over 12 years old: Apply to afected area - do not apply more than 4 times daily. Children 12 years or younger: consult a doctor

Inactive Ingredients

Citrus Fiber, Dimethicone, Isopropyl Alcohol, Jojoba Oil, Phenoxyethanol, Simethicone, Water

* Please review the disclaimer below.