Universal Arthritis And Sport Liquid
FDA Label NDC 52000-301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Universal Distribution Center Llc for the product Universal Arthritis And Sport (NDC 52000-301). 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 drug facts, active ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Methyl Salicylate 0.61%
Capsicum 0.0012%
Purpose
Topical 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
Do not use • other than as directed • on children under 12 years of age
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Directions
• Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
• Children under 12 years of age: ask a doctor
Inactive Ingredients
Isopropyl Alcohol, Magnesium Sulfate, Water
Packaging
52000302-01 (7577102032 1)
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