FDA Label for Neuracin Topical Gel
View Indications, Usage & Precautions
Neuracin Topical Gel Product Label
The following document was submitted to the FDA by the labeler of this product Sola Pharmaceuticals. 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
Camphor 4%
Menthol 10%
Methyl Salicylate 30%
Purpose
Topical Analgesic
Uses
Temporarily relieves minor pain associated with:
- Arthritis
- Simple Backache
- Muscle Strains
- Bruises
- Muscle Sprains
Warnings
For External use only
When using this product
- avoid contact with eyes and mucous membranes
- do no apply to wounds or damaged skin
- do not bandage tightly or use with a heating pad
- use only as directed
Stop use and ask a doctor if condition worsens; symptoms last more than 7 days or clear up and occur again within a few days
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help right away. If pregnant Or Breast-Feeding, Ask A Health Professional Before Use
Directions
- Apply on affected area, not more than 3 to 4 times daily
- Children under 12 years of age; consult a doctor
Other Information
- Store at 20-25°C (68-77°F) Store away from heat
Inactive Ingredients
Benzyl alcohol, Carbomer, Pemulen, Polysorbate 80, Purified Water, Triethanolamine
Package Label.Principal Display Panel
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Neuracin Topical Analgesic Gel
NDC 70512-104-60
Qty 2oz (57G)
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