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Rite aid maximum strength - Medication Information

Product NDC Code 11822-0316
Drug Name

Rite aid maximum strength

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine 20 g/100g
Route ORAL
Dosage Form GEL, DENTIFRICE
RxCUI drug identifier 238910
Application Number M022
Labeler Name Rite Aid
Packages
Package NDC Code Description
11822-0316-4 1 tube in 1 carton (11822-0316-4) / 9 g in 1 tube
11822-0316-3 1 tube in 1 blister pack (11822-0316-3) / 9 g in 1 tube
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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 to open tube, cut tip of tube on score mark adults and children 2 years of age and older: apply to affected area up to 4 times daily or as directed by dentist/doctor children under 12 years of age: adult supervision should be given in the use of this product children under 2 years of age: do not use for denture irritation apply a thin layer to the affected area; do not reinsert dental work until irritation/pain is relieved; rinse mouth well after reinserting

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Blue 1, Carbomer, Flavor, Glycerin, Polyethylene Glycol, Propylene Glycol, Red 40, Sodium Saccharin, Sorbic Acid, Water, Yellow 10

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 temporarily relieves pain associated with mouth and gum irritations

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.
Rite Aid Maximum Strength Benzocaine POLYETHYLENE GLYCOL 400 PROPYLENE GLYCOL SACCHARIN SODIUM SORBIC ACID GLYCERIN FD&C RED NO. 40 D&C YELLOW NO. 10 FD&C BLUE NO. 1 WATER CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED) BENZOCAINE BENZOCAINE Characteristic Mint

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.
RITE AID® PHARMACY MAXIMUM STRENGTH oral pain relief benzocaine 20% anesthetic gel instant pain relief for: toothaches gum pain canker sores denture pain NET WT 0.33 OZ (9 g) RA ORAL ANALGESIC GEL 2824366R2

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts DISTRIBUTED BY: RITE AID, 30 HUNTER LANE CAMP HILL, PA 17011

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 more than directed for more than 7 days unless told to do so by a dentist or doctor 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. In case of overdose, 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 swelling, rash or fever develops irritation, pain or redness persists or worsens symptoms do not improve in 7 days allergic reaction occurs

Storage and handling

Information about safe storage and handling of the drug product.
Other information store at 20-25°C (68-77°F). Do not refrigerate.

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 of 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 more than directed for more than 7 days unless told to do so by a dentist or doctor for teething in children under 2 years of age Stop use and ask a doctor if swelling, rash or fever develops irritation, pain or redness persists or worsens symptoms do not improve in 7 days allergic reaction occurs Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

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