ZENTRIP MOTION SICKNESS- meclizine hydrochloride tablet 
Sato Pharmaceutical Co., LTD

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ZenTrip Motion Sickness (12 Tablets - 25mg each)

Active ingredient (in each tablet)

Meclizine hydrochloride 25mg

Purpose

Antiemetic

Uses

Warnings

Do not use in children under 12 years of age unless directed by a physician

Ask a doctor before use if you have

  • glaucoma
  • a breathing problem such as emphysema or chronic bronchitis
  • difficulty in urination due to enlargement of the prostate gland

Ask a physician or pharmacist before use if you are

  • taking sedatives or tranquilizers

When using this product

  • you may get drowsy
  • be careful when driving a motor vehicle or operating machinery
  • alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverages

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

acesulfame potassium, erythritol, hydroxypropyl cellulose, mannitol, menthol, silicon dioxide colloidal, sodium stearyl fumarate, and yellow ferric oxide.

ZenTrip Motion Sickness - 12Tablets

ZenTrip Motion Sickness - 12Tablets

ZENTRIP MOTION SICKNESS 
meclizine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-805
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
MANNITOL (UNII: 3OWL53L36A)  
MENTHOL (UNII: L7T10EIP3A)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
ERYTHRITOL (UNII: RA96B954X6)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)  
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
Product Characteristics
ColoryellowScorescore with uneven pieces
ShapeROUNDSize13mm
FlavorImprint Code SJ
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49873-805-012 in 1 BOX05/01/2021
16 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00905/01/2021
Labeler - Sato Pharmaceutical Co., LTD (690575642)
Establishment
NameAddressID/FEIBusiness Operations
Sato Pharmaceutical Co., LTD715699133manufacture(49873-805) , pack(49873-805) , label(49873-805)

Revised: 11/2023
Document Id: 0949e5cb-b9e4-cee1-e063-6394a90a5377
Set id: bd86c4c7-b6f0-e3e8-e053-2995a90a4454
Version: 3
Effective Time: 20231103
 
Sato Pharmaceutical Co., LTD