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Tinnitus relinf patches - Medication Information

Product NDC Code 84575-002
Drug Name

Tinnitus relinf patches

Type Brand
Active Ingredients
Borneol .1 g/9g
Camphor, (-)- .1 g/9g
Route TOPICAL
Dosage Form PATCH
Application Number 505G(a)(3)
Labeler Name Linhe Biotechnology (Shenzhen) Co., Ltd
Packages
Package NDC Code Description
84575-002-01 9 g in 1 box (84575-002-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Camphor 0.01% Borneol 0.01%

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.
Adults and children 12 years of age and over: 1.clean and dry affected area. 2.remove patch from film. 3.opply to affected area not morethan 3 to f times daily. 4.remove patch from the skin after at most 8-hour application. Children under 12 years of age: Cansult a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Fu Ling

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 temporary relief of minor aches & pains of muscles 8 joints associated with arthritis, simple backache, strains, bruises, 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.
TINNITUS RELINF PATCHES Camphor, Borneol BORNEOL BORNEOL CAMPHOR, (-)- CAMPHOR, (-)- FU LING

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.
label

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.
1.on damaged skin. 2.with a heating pad. 3.if you are allergic to any ingredients of 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.
lf swallowed, get medical help or contact a Poison Control center right away.

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.
1.skin reactions such as redness, itching, rash, excessive irritation,burning sensation,sweling or blistering occur, 2.symptoms persist for more than 7 days. 3.symptoms clear up and occur 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.
1.use only as directed. 2.avoid contact with the eyes, mucous membranes or rashes. 3.do not bandage tightly.

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