Finafta MultiOral BENZOCAINE DEXTRUM LABORATORIES INC. FDA Approved USES For the temporary relief of occasional minor irritation, pain, sore mouth, pain associated with canker sores or pain due to minor irritation of the mouth and gums cause by dentures or othodontic applicances.
FunFoxMeds box
Substance Benzocaine
Route
ORAL
Applications
M022
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Active Ingredients: (%) Purpose Benzocaine USP 7.5% ................ Oral Anesthetic/Analgesic
Inactive Ingredients
Inactive ingredients : Benzalkonium chloride glycerin methylparaben peppermint oil phosphoric acid propylene glycol propylparaben and purified water.
Strengths
7.5 %
Treats Conditions
Uses For The Temporary Relief Of Occasional Minor Irritation Pain Sore Mouth Pain Associated With Canker Sores Or Pain Due To Minor Irritation Of The Mouth And Gums Cause By Dentures Or Othodontic Applicances

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UNII
U3RSY48JW5
Packaging

label

Package Descriptions
  • label

Overview

USES For the temporary relief of occasional minor irritation, pain, sore mouth, pain associated with canker sores or pain due to minor irritation of the mouth and gums cause by dentures or othodontic applicances.

Indications & Usage

USES For the temporary relief of occasional minor irritation, pain, sore mouth, pain associated with canker sores or pain due to minor irritation of the mouth and gums cause by dentures or othodontic applicances.

Dosage & Administration

DIRECTIONS: For children over 12 years of age and Adults • Apply Finafta® MultiOral Spray up to 4 times daily to affected areas of the mouth, gums or mucus membranes (mouth and throat). Allow to remain in place at least 1 minute and then spit out. • Close bottle tightly after each use. Children under 12 years of age: Do not use.

Warnings & Precautions
Warnings: Do not exceed recommended dosage Methemoglobinemia warning: Use of this product may cause mthemoglobinemia, a serious condition that must be treated promptyly because it reduces the amount of oxygen carried in the blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops: pale, gray, or blue colored skin (cyanosis) headache rapid heart rate shortness of breath dizziness or lightheadedness fatigue or lack of enegry Allegry alert do not use this product if you have a history of allergy to local anesthetics such as prcaine, butacaine, bezocaine, or other "caine" anesthetics. Do not use for teething in children under 2 years of age Consult a doctor promptly if: sore mouth symptoms do not improve in 7 days, or if irritation, pain, or redness persists or worsens. If sore throat is sever, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting.
Purpose

Purpose Oral Anesthetic/Analgesic

Keep Out of Reach of Children

Keep Out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Questions

QUESTIONS OR COMMENTS? 305-805-3456 Monday-Friday (9 a.m.- 5 p.m. EST) www.efficientlabs.com


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