Active Ingredients
Menthol 2.0%
Methyl Salicylate 2.0%
Sincere Pain Relief
FDA Label NDC 70836-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Jiangsu Sincere Pharmaceutical Co., Ltd for the product Sincere Pain Relief (NDC 70836-001). 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 ingredients, purpose, uses, warnings, do not use, directions, inactive ingredients, drug facts, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Menthol Topical Analgesic
Methyl Salicylate Topical Analgesic
Uses
For temporary relief of minor aches and pains of muscles and joints associated with:
Simple backache
Arthritis
Sprains
Strains
Bruises
Warnings
For external use only.
Do Not Use
On wounds or damaged skin.
With Other external analgesic products at the same time.
If you are allergic to any ingredients of this product.
Otherwise than as directed.
Avoid contact with the eyes, mucous membranes or rashes.
Directions
Adults and children 12 years of age and over:
1. Clean and dry the affected areas.
2. Peel off the protective transparent film, paste the gel surface to the affected area.
3. Remove patch from the skin after at most 12 hours' application. The patch works by cold compression. You may feel cold when using.
Children under 12 years of age:
Consult a doctor.
Inactive Ingredients
Sodium Polyacrylate (8000 MW), Glycerin, Polysorbate 80, Tartaric Acid, Water
Drug Facts
Image Description (Carton)
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