Tinnitus Patch
FDA Label NDC 84171-201

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dengzhou Juhetang Medical Equipment Co., Ltd for the product Tinnitus Patch (NDC 84171-201). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Otc - Active Ingredient

→ Otc - Purpose

→ Indications & Usage

→ Warnings

→ Otc - Do Not Use

→ Otc - When Using

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Dosage & Administration

→ Storage And Handling

→ Inactive Ingredient

→ Package Label.principal Display Panel

Other

Tinnitus patch

Otc - Active Ingredient

Lonicera Caprifolium Flower 31%

Otc - Purpose

Topical analgesic

Indications & Usage

Tinnitus Relief Promote blood circulation

Warnings

For external use only

Otc - Do Not Use

with a heating pad
on wounds or damaged skin
if you are allergic to any ingredients of this product

Otc - When Using

use only as directed
do not bandage tightly
avoid contact with the eyes, mucous membranes or rashes

Otc - Stop Use

symptoms persist for more than 7 days
conditions worsen
symptoms clear up and occur again within a few days
Localized,skin,reactions,such
as rash,itching,redness ,pain,swelling and blistering develop