MOTION SICKNESS- meclizine hcl tablet 
Strategic Sourcing Services LLC

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Sunmark 44-403-Delisted

Active ingredient (in each tablet)

Meclizine HCl 25 mg

Purpose

Antiemetic

Uses

for the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness 

Warnings

Do not use

for children under 12 years of age unless directed by a doctor.

Ask a doctor before use if you have

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

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

  • drowsiness may occur
  • avoid alcoholic beverages
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • use caution when driving a motor vehicle or operating machinery

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

corn starch, D&C yellow #10 aluminum lake, lactose anhydrous, magnesium stearate, silicon dioxide

Questions or comments?

Call 1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday

Principal Display Panel

sunmark®

*COMPARE TO DRAMAMINE®
ALL DAY LESS DROWSY
ACTIVE INGREDIENT

NDC 70677-0026-1

Less Drowsy Formula
motion sickness
MECLIZINE HCl 25 mg
Antiemetic

Helps prevent • nausea • vomiting • dizziness
due to motion sickness for up to 24 hours

ACTUAL
SIZE

8 TABLETS

TAMPER EVIDENT: DO NOT USE IF
PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS
ANY SIGNS OF TAMPERING

*This product is not manufactured or
distributed by Medtech Products Inc.,
owner of the registered trademark
Dramamine® All Day Less Drowsy.
50844        REV0219B40319

Distributed by McKesson Corp., via
Strategic Sourcing Services LLC,
Memphis, TN 38141
© 2003 McKesson Corporation
www.sunmarkbrand.com
Money Back Guarantee

Sunmark 44-403

Sunmark 44-403

MOTION SICKNESS 
meclizine hcl tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70677-0026
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
STARCH, CORN (UNII: O8232NY3SJ)  
D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)  
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Product Characteristics
ColoryellowScoreno score
ShapeROUNDSize9mm
FlavorImprint Code 44;403
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70677-0026-11 in 1 CARTON06/24/200212/09/2024
18 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00906/24/200212/09/2024
Labeler - Strategic Sourcing Services LLC (116956644)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(70677-0026)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(70677-0026) , pack(70677-0026)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(70677-0026)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.117025878manufacture(70677-0026)

Revised: 10/2023
Document Id: 1941baf2-1349-4c7b-a1b1-cb8265a24a18
Set id: 48c29625-7ca9-4bcd-8481-475b538b8bae
Version: 8
Effective Time: 20231021
 
Strategic Sourcing Services LLC