KIMITE- scopolamine patch, extended release

KIMITE by

Drug Labeling and Warnings

KIMITE by is a Otc medication manufactured, distributed, or labeled by OASIS TRADING. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Scopolamine

PURPOSE

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KIMITE 
scopolamine patch, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72689-0023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SCOPOLAMINE (UNII: DL48G20X8X) (SCOPOLAMINE - UNII:DL48G20X8X)	SCOPOLAMINE	1.5 mg

Inactive Ingredients
Ingredient Name	Strength
DATURA FEROX WHOLE (UNII: NY0VWX7OX1)
FRANKINCENSE (UNII: R9XLF1R1WM)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
PINELLIA TERNATA WHOLE (UNII: 71T2LKP8GL)
GASTRODIA ELATA TUBER (UNII: 08F85I5YAV)
PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72689-0023-1	2 in 1 BOX; Type 0: Not a Combination Product	11/16/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/15/2018

Labeler - OASIS TRADING (689991468)

Registrant - OASIS TRADING (689991468)

Establishment
Name	Address	ID/FEI	Business Operations
OASIS TRADING		689991468	manufacture(72689-0023)