Kimite
FDA Label NDC 72689-0023

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Oasis Trading for the product Kimite (NDC 72689-0023). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Purpose

Relieve the vomiting, nausea, dizziness, anorexia, and other symptoms resulted from sickness of cars, ships, airplanes, trains and other means of transport

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

■ Tear the protective layer, adhere the adhesive layer to the navel or the back of your ears

■ One/ Two patch per time, accoding to your body condition

■ Attach 10 minutes before the travel, the effect will last about 1-3 days

Warnings

■ Avoid use on allergic and broken skin

■ Not use by pregnant women kid under aged 4

■ Not recommend to use by poorly surgery body

Inactive Ingredient

The abstract of salflower, tall gastrodia tuber, sanchi, hairy datura flower, pinellia tuber, obtuseleaf cinnamon bark, frankincense, dahurian angelica root, bomeol

Dosage & Administration

For external use only

* Please review the disclaimer below.