Active Ingredient
Menthol 15%
Sana Sana Menthol External Analgesic Gel
FDA Label NDC 72367-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Alquimia Najulam S De Rl De Cv for the product Sana Sana Menthol External Analgesic (NDC 72367-000). 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, stop use and ask a doctor if, when using this product, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
External Analgesic
Uses
for the temporary relief of minor aches and pains of muscles and joints associated with
• simple backache
• arthritis
• strains
• bruises
• sprains
Warnings
For external use only
Stop Use And Ask A Doctor If
• condition worsens
• symptoms persist for more than 7 days or clear up and occur again within a few days
When Using This Product
• avoid contact with eyes
• do not apply to wounds or damaged skin
• do not bandage tightly
Keep Out Of Reach Of Children.
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 affected area not more than 3 to 4 times daily
• children under 2 years of age: consult a doctor
Inactive Ingredients
ionized water, glycerin, triethanolamine, carbopol
Package Labeling:
Label (Label)
Label2 (Label2)
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