NeuroMed FA BENZOCAINE SAMBRIA PHARMACEUTICALS, INC. FDA Approved ​Uses For temporary relief of pain and itching due to minor skin irritation.

NEUROMED FA

Generic: BENZOCAINE
Mfr: SAMBRIA PHARMACEUTICALS, INC. FDA OTC
FunFoxMeds box
Substance Benzocaine
Route
TOPICAL
Applications
M017
Product NDC
54723-0722-00 54723-0722-05
Package NDC
54723-722-05

Drug Facts

Composition & Profile

Active Ingredients
​Active Ingredients Benzocaine 20.0% w/w
Inactive Ingredients
​Inactive Ingredients Aqua (Deionized Water) Arnica Montana Flower Extract C13-14 Isoparaffin Caprylic/Capric Triglyceride Cetearetj-25 Chondroitin Sulfate Diethylhexyl Sodium Sulfosuccinate Emu Oil Ethoxydiglycol Ethylhexylglycerin Glucosamine Sulfate Glycerin Isopropyl Palmitate Laureth-7 Melaleuca alternifolia (Tea Tree) Leaf Oil Methylfulfonylmenthane (MSM) Phenoxyethanol Polyacrylamide Polysorbate-20 Safflower Oil Stearic Acid Triethanolamine
Strengths
20.0 %
Treats Conditions
Uses For Temporary Relief Of Pain And Itching Due To Minor Skin Irritation

Identifiers & Packaging

Container Type UNKNOWN
NDC 54723-0722-00
All Product Codes
54723-0722-00 54723-0722-05
UNII
U3RSY48JW5
SPL Set IDs
97345ed4-51c3-4221-852c-2cd563f33317
Packaging

Product label Packet die cut

Package Descriptions
  • Product label Packet die cut
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 then 3 or 4 times daily. Children under 2 years of age: consult a physician.

Warnings & Precautions
​Warnings ​For external use only Avoid contact with eyes
Purpose

​Purpose External Analgesic

Stop Use & Ask a Doctor

​Stop use and ask doctor if ​ • Condition worsens, or if symptoms persist for more then 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. 54723-668-03 800-759-6876

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