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Product NDC Code | 82739-021 | ||||
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Drug Name | Treatonic tattoo numbing cream |
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Type | Brand | ||||
Pharm Class | Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE] |
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Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | CREAM | ||||
RxCUI drug identifier | 1421893 | ||||
Application Number | M017 | ||||
Labeler Name | Shenzhen Situya Trading Co., Ltd. | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient LIDOCAINE 4%
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 For adults: ■ Cleanse, Rinse, and dry the affected area with warm water. ■ Apply a thick numbing cream onto the treated area. ■ Apply up to 6 times a day. For children under 12 years of age: ■ Consult a doctor for guidance.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Carbomer 934, Emu Oil, Arnica, Lecithin(Soybean), Propylene Glycol, Tocopheryl Acetate, Benzyl Alcohol, 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 temporary ease local discomfort, itching, soreness, or burning in the perianal area associated with anorectal disorders.
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.Treatonic Tattoo Numbing Cream Tattoo Numbing Cream LECITHIN, SOYBEAN ARNICA MONTANA PROPYLENE GLYCOL .ALPHA.-TOCOPHEROL ACETATE LIDOCAINE LIDOCAINE EMU OIL BENZYL ALCOHOL CARBOMER 934 WATER
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
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 ■ if discomfort persists for 7 days. ■ The symptoms being treated do not subside or if redness irritation swelling, pain, or other symptoms develop or increase.
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, if there is any allergic reaction to this product. ■ In case of accidental overdose, get medical help, or contact the poison control center immediately.
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 and avoid contact with eyes. In case of accidental ingestion, seek medical attention immediately
Questions
A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.Questions [email protected]
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
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 ■ Only take the recommended daily dosage unless otherwise instructed by a doctor. ■ Some individuals may experience allergic reactions to the ingredients contained in this product. ■ Never put it into the rectum by using the finger or any medical devices.
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