FDA Label for Oxyrub Pain Relief
View Indications, Usage & Precautions
Oxyrub Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Pure Source, 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 Ingredient
Menthol (1.25%)
Purpose
Topical Analgesic
Uses
temporarily relieves minor aches and pains of muscles and joints associated
- simple backaches
- arthritis
- strains
- sprains
- bruises
Warnings
For external use only.
- Use only as directed.
- with a heating pad, may blister skin
- on open wounds or damaged skin
- Avoid contact with eyes
- Do not bandage tightly
- skin redness or excessive skin irritation develops
- condition worsens or symptoms persist for more than 7 days
- symptoms clear up and occur again in a few days
Do not use
Ask a doctor before use if you have redness over the affected area
When using this product
Stop use and consult a doctor if
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 no more than 3-4 times daily.
Children under 12 years of age, consult a doctor.
Other Information
Store at room temperature. For Lot Number and Expiration Date, see crimp at end of tube.
Inactive Ingredients
Bitter Orange Oil, C13-14 Isoparaffin, Caprylhydroxomic Acid, Caprylyl Glycol, Eucalyptus Oil, Glycerin, Laureth-7, Oxidized Corn Oil, Polyacrylamide (1000 MW), Polysorbate 20, Water
Oxyrub Pain Relief Cream 4Oz/114G (65121-113-04)
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