NeuroMed Topical Anesthetic 7 LIDOCAINE HYDROCHLORIDE SAMBRIA PHARMACEUTICALS FDA Approved Uses For temporary relief of pain and itching due to minor skin irritation.
FunFoxMeds box
Route
TOPICAL
Applications
M017
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Active Ingredient Lidocaine HCL 4.00% w/w Purpose External Analgesic
Inactive Ingredients
Inactive Ingredients Aqua (Deionized Water) Arnica Montana Flower Extract C13-14 Isoparaffin Chrondroitin Sulfate Emu Oil Ethoxydiglycol Ethylhexyglycerin Glucosamine Sulfate Isopropyl Palmitate Laureth-7 Melaleuca Alternifolia (Tea Tree) Oil Methylsulfonylmethane (MSM) Phenoxyethanol Polyacrylamide Propylene Glycol Stearic Acid Triethanolamine.
Strengths
4.00 %
Treats Conditions
Uses For Temporary Relief Of Pain And Itching Due To Minor Skin Irritation

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UNII
V13007Z41A
Packaging

Product label die cut Packet

Package Descriptions
  • Product label die cut Packet

Overview

Uses For temporary relief of pain and itching due to minor skin irritation.

Indications & Usage

Uses For temporary relief of pain and itching due to minor skin irritation.

Dosage & Administration

Directions For adults and children two-years or older: Apply to affected area not more than 3 or 4 times daily. Children under 2 years of age: consult a physician. Apply in a circular motion for 50 to 60 seconds.

Warnings & Precautions
Warnings ​For external use only ​ ​Avoid contact with eyes ​Do not use ​ in large quantities, particularly over raw surfaces or blistered areas
Purpose

Purpose External Analgesic

Do Not Use

​Do not use ​ in large quantities, particularly over raw surfaces or blistered areas

Stop Use & Ask a Doctor

​Stop use and ask a doctor if ​ • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Discontinue use.

Keep Out of Reach of Children

​Keep out of reach of children ​ • If product is swallowed, get medical help or contact a Poison Control Center right away.

Questions

​Questions or Comments? FDA Registered: NDC No. 54723-667-04 800-759-6876


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