FDA Label for Ubredol
View Indications, Usage & Precautions
Ubredol Product Label
The following document was submitted to the FDA by the labeler of this product Pharmadel 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.
Otc - Purpose
Active ingredient | Purpose |
Methyl salicylate 10% .................. | 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. Avoid contact with the eyes.
Do Not
- apply on wounds or irritated skin
- bandage tightly
Stop Use And Ask Doctor Immediately If
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again within a few days
If Pregnant Or Breast-Feeding,
ask a health care professional before use.
Keep Out Of Reach Of Children.
If swallowed get medical help, or contact a Poison Control Center immediately.
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: do not use, consult a doctor
Other Information
- store between 59°- 86°F (15 - 30°C)
- do not use if clear seal over jar is broken, torn or missing
Inactive Ingredients
camphor, D&C yellow #11, eucalyptus oil, lanolin oil, levomenthol, mineral oil, petrolatum, propylparaben, tea tree oil
Distributed By:
Pharmadel LLC
New Castle, DE 19720
+1-866-359-3478
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