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Gumnumb topical anesthetic - Medication Information

Product NDC Code 24794-220
Drug Name

Gumnumb topical anesthetic

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine 200 mg/g
Route DENTAL
Dosage Form GEL
RxCUI drug identifier 238910,
645497
Application Number part356
Labeler Name Crosstex International Inc.
Packages
Package NDC Code Description
24794-220-30 30 g in 1 jar (24794-220-30)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient (in each gram) Benzocaine 200mg

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 Apply only amount needed to the oral mucosa to prevent or relieve pain. children under 2 years of age: do not use

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients flavoring, PEG 3350, PEG 400, sodium saccharin. May contain blue #1, green #3, green #5, red #3, red #28, red #40, yellow #5, (tartrazine), yellow #6, as a color additive.

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.
Use For oral mucosa use only, as directed by dentist. For the temporary relief of pain due to minor dental procedures.

Purpose

Information about the drug product’s indications for use.
Purpose Oral Anesthetic

Spl product data elements

Usually a list of ingredients in a drug product.
Gumnumb Topical Anesthetic Benzocaine POLYETHYLENE GLYCOL 3350 POLYETHYLENE GLYCOL 400 SACCHARIN SODIUM FD&C YELLOW NO. 5 FD&C YELLOW NO. 6 FD&C RED NO. 3 FD&C RED NO. 40 FD&C BLUE NO. 1 FD&C GREEN NO. 3 D&C RED NO. 28 D&C GREEN NO. 5 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.
Gum Numb Cherry Rev 7 OL_newnumber.jpg

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.

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? [email protected] or www.crosstex.com

Storage and handling

Information about safe storage and handling of the drug product.
Other Information Store at 59° - 86°F (15°-30°C). Protect from freezing.

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 Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly 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 energy Allergy Alert: Do not use on patients with a history of allergies to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics. Do not use for more than 7 days unless directed by a physician. If sore mouth symptoms do not improve in 7 days; irritation, pain, or redness persists or worsens; or if swelling, rash or fever develops, see your physician promptly. for teething in children under 2 years of age When using this product Avoid contact with eyes. If contact occurs, flush with water. Do not exceed recommended dosage. If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast feeding, ask a physician before use.

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

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