FDA Label for Doloflex Pain Relief
View Indications, Usage & Precautions
Doloflex Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product United Health & Beauty Corp. 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 - Active Ingredient
Camphor 1.5%, Menthol 2%, Methyl Salicylate 3
Otc - Purpose
Topical Analgesic
Indications & Usage
Temporarily relieves the minor aches and pain of muscles and joints associated with simple backache, arthritis, strains, sprains, and bruises.
Warnings
For external use only.
Do not use on children under 12 years of age, with a heating pad (may blister skin), on wounds or damaged skin.
When using this product do not bandage tightly, avoid contact with the eyes or mucous membranes.
Stop use and ask a doctor if excessive irritation develops, symptoms last more than 7 days or clear up and occur again within a few days, condition worsens.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a poison control center right away.
Dosage & Administration
Adults and children 12 years of age or older: apply to affected area up to 3 to 4 times daily. Children under 12 years of age: consult a physician.
Inactive Ingredient
Water, alcohol, carbomer, DMDM Hydantoin, Iodopropynyl Butylcarbamate, PEG-40 Hydrogenated Caster Oil, Aesculus Hippocastanum Seed Extract, Centella Assiatica Leaf Extract, Arnica Montana Flowers Oil, Calendula Officinalis Flower Extract, Triethanolamine.
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