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Red cross oral pain relief - Medication Information

Product NDC Code 10742-8902
Drug Name

Red cross oral pain relief

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine 200 mg/ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 308657
Application Number part356
Labeler Name The Mentholatum Company
Packages
Package NDC Code Description
10742-8902-1 1 bottle in 1 blister pack (10742-8902-1) / 3.7 ml in 1 bottle
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Benzocaine 20%

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 using tweezers, immerse cotton pellet in medication apply pellet to affected area, then remove adults and children 2 years and over: use up to 4 times daily or as directed by a dentist or doctor children under 12 years: supervise while using this product children under 2 years: do not use

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients ammonium glycyrrhizate, flavor, polyethylene glycol, propylene glycol, saccharin calcium

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 temporarily relieves pain associated with ▪ toothache ▪ canker sores ▪ minor mouth irritation or injury of the mouth and gums caused by dentures or braces

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Red Cross Oral Pain Relief benzocaine AMMONIUM GLYCYRRHIZATE POLYETHYLENE GLYCOL 400 PROPYLENE GLYCOL SACCHARIN CALCIUM 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.
Package/Label Principal Display Panel Red Cross Oral Pail Oral Anesthetic Principal Display Panel Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do Not Use for teething in children under 2 years of age

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 more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away.

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 a doctor if sore mouth symptoms do not improve in 7 days swelling, rash, or fever develops irritation, pain, or redness persists or worsens

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product do not use for more than 7 days unless directed by a dentist or doctor do not exceed recommended dosage

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 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 this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other “caine” anesthetics Do Not Use for teething in children under 2 years of age When using this product do not use for more than 7 days unless directed by a dentist or doctor do not exceed recommended dosage Stop use and ask a doctor if sore mouth symptoms do not improve in 7 days swelling, rash, or fever develops irritation, pain, or redness persists or worsens

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