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Prinumb tattoo numbing cream - Medication Information

Product NDC Code 84555-001
Drug Name

Prinumb tattoo numbing cream

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine 5 g/100ml
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 1534792
Application Number M017
Labeler Name Shijiazhuang Auro Technology Co., Ltd.
Packages
Package NDC Code Description
84555-001-01 50 ml in 1 bottle (84555-001-01)
84555-001-02 100 ml in 1 bottle (84555-001-02)
84555-001-03 150 ml in 1 bottle (84555-001-03)
84555-001-04 200 ml in 1 bottle (84555-001-04)
84555-001-05 30 ml in 1 tube (84555-001-05)
84555-001-06 60 ml in 1 tube (84555-001-06)
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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.
Directions Apply up to 3 times a day. Children (under 12 years of age): consult a doctor. Adults: before applying this product, clean the affected area with mild soap and warm water and rinse thoroughly. Pat dry the area with a soft cloth or tissue.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients .Alpha.-Tocopherol Acetate Carbomer 940 Chrysanthemum Extract Glycerol, Lecithin, Soybean Portulaca Oleracea Extract Prilocaine Propylene Glycol Sodium Hyaluronate 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.
Use For temporarily relieves pain and itching associated with minor burns, minor cuts or skin irritations

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Prinumb Tattoo Numbing Cream Tattoo Numbing Cream PROPYLENE GLYCOL LIDOCAINE LIDOCAINE CHRYSANTHEMUM INDICUM WHOLE PRILOCAINE CARBOMER 940 GLYCERIN .ALPHA.-TOCOPHEROL ACETATE LECITHIN, SOYBEAN WATER PURSLANE HYALURONATE SODIUM

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.
PRINCIPAL DISPLAY PANEL 1 2 3 4 5

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask Doctor discomfort persists for 7 days.

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 Pregnant or breastfeeding, ask your doctor before use. in case of accidental overdose, seek immediate medical help or contact the Poison Control Center. seal is broken or missing.

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 Oot Of Reach Of Children Avoid contact with the eyes.If swallowed,seek medical attention 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 The symptom being treated does not improve, or if redness, irritation, swelling, pain, or other symptoms appear or worsen. Seek medical help right away.

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 Do not exceed the recommended daily dosage unless directed by a doctor. Certain persons can develop allergic reactions to ingredients in this product. Do not put this product into the rectum by using fingers or any medical device or applicator.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store at room temperature and out of direct sunlight or heat.

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 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