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Myderm medical 5 lidocaine numbing roll-on - Medication Information

Product NDC Code 72667-072
Drug Name

Myderm medical 5 lidocaine numbing roll-on

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine 5 g/100g
Route TOPICAL
Dosage Form STICK
Application Number M015
Labeler Name Inspec Solutions
Packages
Package NDC Code Description
72667-072-01 89 g in 1 bottle, plastic (72667-072-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Lidocaine 5%

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.
Apply to affected area not more than 3 to 4 times daily

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Acrylates/C10-30 Alkyl Acrylate Crosspolymer Aloe Vera Barbadensis Leaft Juice Inactive ingredients 2-animo-2methyl-1propanol 2-Methylamino-2-methyl-1-propanol Cetearyl Alcohol Citric Acid Dimethicone Disodium EDTA Ethanol Ethyhexylglycerin Glyceril Stearate Phenoxyethanol Potassium Sorbate Silicone Gel Sodium Benzoate Steareth-21 Water

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.
For external use only

Purpose

Information about the drug product’s indications for use.
Lidocaine 5% ------------------------------------------------------------Local Anesthetic

Spl product data elements

Usually a list of ingredients in a drug product.
MyDerm Medical 5 Lidocaine Numbing Roll-On Lidocaine AMINOMETHYLPROPANOL DIMETHICONE 100 POTASSIUM SORBATE ALOE VERA LEAF CAPRYLYL TRISILOXANE GLYCERYL MONOSTEARATE PHENOXYETHANOL ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) ALCOHOL ETHYLHEXYLGLYCERIN CITRIC ACID ACETATE MAGNESIUM DISODIUM EDTA SODIUM BENZOATE LIDOCAINE LIDOCAINE CETOSTEARYL ALCOHOL STEARETH-21

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.
MyDerm 5 Lidocaine

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 swallowed, get medical help or contact a Poison Control Center immediately.

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 doctor if condition worsens, or symtoms persist for more than 7 days,or clear up and reoccur again within a few days.

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 avoid conatct with the eyes or muccous membranes.

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.
For external use only.

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