FDA Label for Uriflex Fast Acting Analgesic Pain Relief
View Indications, Usage & Precautions
Uriflex Fast Acting Analgesic Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Rejuvica Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredients
Menthol 4.50%
Purposes
External Analgesic
Uses:
For temporary relief of minor aches and pains associated with simple backache, arthritis, bruises, sprains, and strains.
Warnings:
For External Use Only. Avoid Contact With Eyes.
Do Not Apply
to Open Wounds or Damaged Skin. If symptoms persist for more than seven days, discontinue use and consult physician.
Keep Out Of Reach Of Children.
If swallowed, consult physician. Do not bandage tightly.
If Pregnant Or Breast Feeding,
contact physician prior to use.
Directions:
Apply directly to affected area. Do not use more than four times per day.
Other Ingredients:
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Cetyl Alcohol, Diazolidinyl Urea, Isopropyl Myristate, Methyl Paraben, Methyl Salicylate, PEG-8, Propyl Paraber, Propylene Glycol, Sodium Laruyl Sulfate, Triethanolamine.
Package Labeling:
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