Drugplain

Neuracin Topical Gel 40 mg/g

Neuracin Topical Analgesic Gel · GEL · SOLA Pharmaceuticals

No Recall History
Plain English

Neuracin Topical Gel is an over-the-counter pain relief medication applied directly to the skin at a strength of 40 mg/g. It is used to temporarily relieve minor aches and pains in muscles and joints.

Key Facts

Brand Name
Neuracin Topical Gel
Generic Name
Neuracin Topical Analgesic Gel
NDC Code (Product)
70512-104
Manufacturer
SOLA Pharmaceuticals
Strength
40 mg/g
Dosage Form
GEL
Route
TOPICAL
Marketing Status
Application #
M017
Marketing Start
05/24/2021

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Temporarily relieves minor pain associated with: Arthritis Simple Backache Muscle Strains Bruises Muscle Sprains

Dosage & Administration

Directions Apply on affected area, not more than 3 to 4 times daily Children under 12 years of age; consult a doctor

Warnings

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

Frequently Asked Questions

What is Neuracin Topical Gel used for?

Neuracin Topical Gel is an over-the-counter pain relief medication applied directly to the skin at a strength of 40 mg/g. It is used to temporarily relieve minor aches and pains in muscles and joints.

Is Neuracin Topical Gel a controlled substance?

Neuracin Topical Gel is not classified as a controlled substance by the DEA.

What is the generic name for Neuracin Topical Gel?

The generic name for Neuracin Topical Gel is Neuracin Topical Analgesic Gel. There are no other listed brand versions of Neuracin Topical Analgesic Gel.

What is the NDC code for Neuracin Topical Gel 40 mg/g?

The NDC (National Drug Code) for Neuracin Topical Gel 40 mg/g is 70512-104, listed by SOLA Pharmaceuticals.

Product NDC

70512-104

Package NDC

70512-104-60

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)