MOTION SICKNESS- motion sickness patch patch

motion sickness by

Drug Labeling and Warnings

motion sickness by is a Otc medication manufactured, distributed, or labeled by Zhengzhou Zhuoqing Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Menthol 2%

Purpose

Refreshing

Uses

temporarily relieves these symptoms due to motion.

vomiting nauseas dizziness

Warnings

Warnings : For external use only.

Ask a doctor before use if you have

1 . Not recommended for children under 4 years of age

2 . Do not use on allergic , wounds or damaged skin

Ask adoctor or phamacistbefore use if you are taking tranquilizers or sedatives

Do not use

When using this product. Do not use this product if you have heart disease , high blood pressurethyroid disease , diabetes . unless directed by a doctor . Ask a doctor or pharmacist before use if you are presently taking aprescription drug for high blood pressure or depression

WHEN USING

When using this product. Do not use this product if you have heart disease , high blood pressurethyroid disease , diabetes . unless directed by a doctor . Ask a doctor or pharmacist before use if you are presently taking aprescription drug for high blood pressure or depression

STOP USE

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. in case of Excessive use , get help from a health professional right away

Directions

1 . Remove the protective layer , apply the patch behind the earsand on the belly button at the same time if motion sickness serious

2 . Please use it ten minutes before travel , The effectcan last for1 to 3 days

Other information

Store in a cool dry place away for direct sunlight

Inactive ingredients

PTFE , Borneol , Wormwood , Non-woven fabric ,Pressure sensitive adhesive for medical purposes , A combination of chitin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOTION SICKNESS 
motion sickness patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83632-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2 g  in 100

Inactive Ingredients
Ingredient Name	Strength
BORNEOL (UNII: M89NIB437X)
GINGER (UNII: C5529G5JPQ)
POLYTETRAFLUOROETHYLENE (UNII: E1NC1JVS3O)
CHITIN (UNII: 8SH93A7QWW)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83632-001-01	24 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
2	NDC: 83632-001-02	36 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
3	NDC: 83632-001-03	48 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
4	NDC: 83632-001-04	10 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
5	NDC: 83632-001-05	20 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
6	NDC: 83632-001-06	30 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
7	NDC: 83632-001-07	10 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
8	NDC: 83632-001-08	20 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
9	NDC: 83632-001-09	30 in 1 BOX; Type 0: Not a Combination Product	08/16/2023
10	NDC: 83632-001-10	40 in 1 BOX; Type 0: Not a Combination Product	08/16/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/16/2023

Labeler - Zhengzhou Zhuoqing Trading Co., Ltd. (713814647)

Establishment
Name	Address	ID/FEI	Business Operations
Zhengzhou Zhuoqing Trading Co., Ltd.		713814647	manufacture(83632-001)