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Product NDC Code | 79740-009 | ||||
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Drug Name | Tidl pain relief numbing tidl |
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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 | PATCH | ||||
RxCUI drug identifier | 1649008 | ||||
Application Number | M017 | ||||
Labeler Name | The Anthos Group | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Lidocaine 4%, Menthol 3%
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.one slice at a time
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Purity Water, 059QF0KO0R Glycerol, PDC6A3C0OX Sodium polyacrylate, 05I15JNI2J Wintergreen Oil, LAV5U5022Y Ethanol, 3K9958V90M Tartaric acid, W4888I119H Aluminum Glycinate, 1K713C615K Chilli extract, 00UK7646FG EDTA-2NA, 9G34HU7RV0
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.Uses Temporary relief from minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and sprains
Purpose
Information about the drug product’s indications for use.Topical Analgesic
Spl product data elements
Usually a list of ingredients in a drug product.TIDL PAIN RELIEF NUMBING TIDL PAIN RELIEF GLYCERIN SODIUM POLYACRYLATE (2500000 MW) METHYL SALICYLATE ALCOHOL TARTARIC ACID DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS CAPSICUM WATER EDETIC ACID MENTHOL MENTHOL LIDOCAINE LIDOCAINE
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.79740-009-1 5 BAG in 1 BOX 79740-009-2 1 PATCH in 1 BAG 79740-009-1 5 BAG in 1 BOX 79740-009-2 1 PATCH in 1 BAG
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.Wamings For extemal use only . Do not use a on puncture wounds , cuts , imitated , damaged or swollen skin more than 1 path on your body at a time or with other topical analgesics at the same time with a heating pad or apply local heat to the area of use When using his product use only as directed do not bandage tighty avoid contact with eyes and mucous membranes rare cases of serous bums have been reported with products of this type a transient buming sensation may occur upon application but enerally disappears in several days dispose of used patch in manner hat always keeps products away from children and pets . Used patches still contain e g po at can po s ad fs f a hid or pt chews or ingests this patch Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days symptoms ear up and occur again within a few days severe burning sensation, redness or irritation develops you experience signs of skin inur , such as pain , sw , or blistering where the product was appliedIf pregnant or breast-feeing , ask a health professional efore use . ep out of each of hilden .If swallowed , get medical help or contact a Poison Control Center night 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