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4x medicated toothache and gum gel - Medication Information

Product NDC Code 56062-312
Drug Name

4x medicated toothache and gum gel

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Copper Absorption Inhibitor [EPC],
Decreased Copper Ion Absorption [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzalkonium chloride .13 g/100g
Benzocaine 20 g/100g
Menthol .5 g/100g
Zinc chloride .15 g/100g
Route ORAL
Dosage Form GEL, DENTIFRICE
RxCUI drug identifier 2369638
Application Number M022
Labeler Name Publix Super Markets INC
Packages
Package NDC Code Description
56062-312-22 1 tube in 1 carton (56062-312-22) / 7 g in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Benzalkonium chloride 0.13% Benzocaine 20% Menthol 0.5% Zinc Chloride 0.15%

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 cut open tip of tube on score mark adults and children 2 years of age and older: apply a small amount of product to the cavity and around the gum surrounding the teeth. Use up to 4 times daily or as directed by a dentist or doctor. children between 2 and 12 years of age: ask a doctor before use. Should be supervised in the use of this product children under 2 years of age: do not use do not use if tip is cut prior to opening * this preparation is intended for use in cases of toothache, only as a temporary expedient until a dentist can be consulted *do not use continuously *this formula will stay in place for extended duration of relief *avoid using toothpaste or drinking soft drinks or fruit juices for at least one hour after applying

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
ammonium glycyrrhizate, blue 1, flavor, PEG-8, PEG-75, sodium saccharin, sorbic acid

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.
temporary relief of pain due to toothache * to help protect against infection of minor oral irritation

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
4x Medicated Toothache and Gum Gel Benzocaine POLYETHYLENE GLYCOL 3350 FD&C BLUE NO. 1 BENZOCAINE BENZOCAINE SORBIC ACID BENZALKONIUM CHLORIDE BENZALKONIUM POLYETHYLENE GLYCOL 400 METHYL SALICYLATE SACCHARIN SODIUM ZINC CHLORIDE ZINC CATION AMMONIUM GLYCYRRHIZATE MENTHOL MENTHOL blue to Blue Green

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.
PUBLIX SUPER MARKETS, INC 4X MEDICATED GEL TOOTHACHE & GUM PAIN RELIEF 20% Benzocaine to relieve oral pain Kills harmful bacteria Astringent to help prevent infection Cools gum & relieves irritation Compare to the active ingredients in Orajel 4X medicated for toothache & Gum gel* NET WT 0.25OZ (7 g) Publix 4X Medicated Toothache & Gum Gel

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: PUBLIX SUPER MARKETS, 3300 PUBLIX CORPORATE PARKWAY LAKELAND, FL 33811

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 directed 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 or allergic reaction, 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

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.
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 lightheadness fatique or lack of energy Alergy 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

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