Otc - Active Ingredient
Methyl salicylate
L-Menthol
dl-Camphor
Zenol Double Action Patch
FDA Label NDC 87520-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ba Trade Inc for the product Zenol Double Action (NDC 87520-0002). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Kaolin
Zinc oxide
Titanium oxide
Gelatin
Glycerin
Liquid paraffin
Polybutene
Sodium polyacrylate
Rubber Latex
Purified Water
Otc - Purpose
For temporary relief of minor aches & pains of muscles & joints
Associated with: Arthritis, Simple backache, Strains, Bruises, Sprains
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Adults and children 12 years of age and over:
Clean and dry affected area
Remove patch from film
Apply to affected area not more than 3 to 4 times daily
Remove patch from the skin after at most 8-hour application
Children under 12 years of age:
Consult a doctor
Warnings
For external use only
Use only as directed
Avoid contact with eyes, mucous membranes or rashes
Do not bandage tightly
Dosage & Administration
for external use only
* Please review the disclaimer below.
