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Zhuanggu gao pain relieving - Medication Information

Product NDC Code 68007-402
Drug Name

Zhuanggu gao pain relieving

Type Brand
Active Ingredients
Menthol 35 mg/1
Route TRANSDERMAL
Dosage Form PLASTER
RxCUI drug identifier 2566787
Application Number part348
Labeler Name GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD
Packages
Package NDC Code Description
68007-402-01 2 pouch in 1 box (68007-402-01) / 5 plaster in 1 pouch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Menthol 3.5%

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 ■ adults and children 2 years of age and older: remove the protective film from the plaster. Apply to affected area not more than 3 to 4 times daily. ■ children under 2 years of age: consult your physician.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients angelica sinensis root, cang-zhu atractylodes rhizome, fragrant angelica root, ginger rhizome, kaempferia galanga rhizome, lanolin, mineral oil, petrolatum, rosin, rubber, star anise fruit, styrene-isoprene, and zinc oxide on a fabric backing covered with protective paper film.

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 For the temporary relief of minor aches and pains of muscles and joints due to: ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Purpose

Information about the drug product’s indications for use.
Purpose External Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Zhuanggu Gao Pain Relieving Menthol MENTHOL MENTHOL ANGELICA SINENSIS ROOT ATRACTYLODES LANCEA ROOT ANGELICA DAHURICA ROOT GINGER KAEMPFERIA GALANGA ROOT LANOLIN MINERAL OIL PETROLATUM ROSIN NATURAL LATEX RUBBER STAR ANISE FRUIT STYRENE ISOPRENE ZINC OXIDE

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.
Zhuanggu Gao Pain Relieving Plaster NDC 68007-402-01 10 Patches Each Patch 2.75 in x 4 in (7 cm x 10 cm) 5 Patches per Pouch IMAGE OF BOX

Ask doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a doctor or pharmacist before use if you have ■ any concerns about using this product

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 ■ on wounds ■ on irritated or damaged skin ■ if you are allergic to any ingredient in this product

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 to avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? (888) 221-3496 M-F 9 am to 5 pm ■ you may also report serious side effects to this phone number

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 ■ condition worsens ■ symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ excessive irritation of the skin develops ■ nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs ■ you feel actual pain or experience blistering or burning after application (it is normal to feel a warming or cooling sensation) ■ when using for pain of arthritis: ■ pain persists for more than 10 days ■ redness is present ■ in conditions affecting children under 12 years of age

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 contact with the eyes or mucous membranes ■ do not bandage tightly ■ do not apply heat to the area in form of heating pads, hot water bottles, or lamps (doing so increases the risk of serious burns) ■ avoid placing on extremely hairy areas of skin to avoid irritation upon removing the plaster

Storage and handling

Information about safe storage and handling of the drug product.
Other information ■ keep plasters tightly closed in the zip-lock pouch ■ store at 15 to 30 C (59 to 86 F) in a dry place away from sunlight

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 Allergy alert: This product contains natural rubber latex which may cause allergic reactions.

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