Active Ingredients
Camphor 9%
Menthol 16%
Medicated Balm Arthritis Pain Relieving Cream
FDA Label NDC 51367-032
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by International Nature Nutraceuticals Inc. for the product Medicated Balm Arthritis Pain Relieving Cream (NDC 51367-032). 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, uses, warnings, do not use:, stop using and consult with doctor if:, other information, directions, 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
Uses
The temporary relief of minor aches and pains of muscles and joints due to:
Simple backache
Sprains
Bruises
Arthritis
Warnings
For External use only
Do Not Use:
On wound or damaged skin
Otherwise than as directed
Stop Using And Consult With Doctor If:
Condition worsens
symptoms persist for more than 7 days or clear up and occur again within a few days
allergic to salicylates or aspirin
Other Information
Keep bottle tightly closed, store in a cool and dry place
Do not use if seal is broken
Directions
Adults and children 2 years of age and older: Apply to affected area 3-4 times daily
Children under 2 years of age: Do not use, consult a doctor
Keep Out Of Reach Of Children
In case of accidental ingestion, contact a doctor or poision control center immediately
Inactive Ingreidents
Eucalyptus oil
Petrolatum
Cinnamon bark oil
Paraffin
Ceresin
Peppermint oil
Pregnant Or Lactating Women
Consult a doctor before using
When Using This Product
Avoid contact with the eyes, mouth, or mucous membranes
Do not bandage tightly
Packaging
Image Description (Package)
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