Nan San Musflex External Analgesic
FDA Label NDC 55424-1238

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Chung Kee Usa International Inc for the product Nan San Musflex External Analgesic (NDC 55424-1238). 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, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Camphor 6%

Menthol 16%

Purpose

External Analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

Warnings

For external use only.

Avoid contact with the eyes.

If Pregnant Or Breast-Feeding

ask a health professional before use.

Keep Out Of Reach Of Children To Prevent Accidental Poisoning.

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily
  • Children under 2 years of age: Consult a physician

Other Information

  • Store at room temperature under 85 degrees F (30 degrees C)

Inactive Ingredients

Oleum Cinnamoni, Oleum Eucalypti,  Oleum Ocimi Gratissimi, Wintergreen Oil

Manufactured By:

Nan San (HK) Pharmaceutical Factory Limited

Unit C1, 10/f, Hoi Bun

Industrial Building, 6 Wing Yip Street,

Kwun Tong, Hong Kong, China.

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