Active Ingredients
Camphor 4%
Menthol 10%
Methyl Salicylate 30%
Neuracin Topical Gel
FDA Label NDC 70512-104
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sola Pharmaceuticals for the product Neuracin Topical Gel (NDC 70512-104). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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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