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Neuromed fa - Medication Information

Product NDC Code 54723-722
Drug Name

Neuromed fa

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine 20 mg/100mg
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 723562
Application Number M017
Labeler Name Sambria Pharmaceuticals, Inc.
Packages
Package NDC Code Description
54723-722-05 5000 mg in 1 packet (54723-722-05)
54723-722-03 3000 mg in 1 packet (54723-722-03)
54723-722-04 1500 mg in 1 packet (54723-722-04)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
​Active Ingredients Benzocaine 20.0% w/w

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
​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.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
​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

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
​Uses For temporary relief of pain and itching due to minor skin irritation.

Purpose

Information about the drug product’s indications for use.
​Purpose External Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
NeuroMed FA Benzocaine WATER ARNICA MONTANA FLOWER C13-14 ISOPARAFFIN MEDIUM-CHAIN TRIGLYCERIDES CETEARETH-25 CHONDROITIN SULFATE SODIUM (BOVINE) DOCUSATE SODIUM EMU OIL DIETHYLENE GLYCOL MONOETHYL ETHER ETHYLHEXYLGLYCERIN GLUCOSAMINE SULFATE GLYCERIN ISOPROPYL PALMITATE LAURETH-7 MELALEUCA ALTERNIFOLIA LEAF DIMETHYL SULFONE PHENOXYETHANOL POLYACRYLAMIDE (10000 MW) POLYSORBATE 20 SAFFLOWER OIL STEARIC ACID TROLAMINE BENZOCAINE BENZOCAINE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Product label image description image description

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
​Keep out of reach of children ​ • If product is swallowed, get medical help or contact a Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
​Other Information Protect this product from excessive heat or direct sun.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
​Questions or Comments? FDA Registered: NDC No. 54723-668-03 800-759-6876

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
​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.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
​Warnings ​For external use only Avoid contact with eyes

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API