MOTION SICKNESS- meclizine hcl tablet 
H E B

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HEB 44-403

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

colloidal silicon dioxide, D&C yellow #10 aluminum lake, lactose monohydrate, magnesium stearate, pregelatinized starch

Questions or comments?

1-800-426-9391

Principal Display Panel

H-E-B®

NDC 37808-903-12

Compare to
Dramamine®
Less Drowsy
active ingredient*

Motion
Sickness
Meclizine HCl 25 mg

Antiemetic

Helps prevent Nausea
& Dizziness due to
Motion Sickness for
up to 24 hours

•For Ages 12 and Over
•24 Hours of Protection
• Less Drowsy Formula

Actual
Size

100 TABLETS

TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

*This product is not manufactured or distributed by
Medtech Products Inc., owner of the registered trademark
Dramamine® Less Drowsy.
50844   ORG042340312

100%
GUARANTEE
promise

MADE WITH PRIDE AND
CARE FOR H-E-B®,
SAN ANTONIO, TX 78204

HEB 44-403A

HEB 44-403A

MOTION SICKNESS 
meclizine hcl tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-903
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
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
ColoryellowScoreno score
ShapeROUNDSize9mm
FlavorImprint Code 44;403
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-903-12100 in 1 BOTTLE; Type 0: Not a Combination Product06/24/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00906/24/2019
Labeler - H E B (007924756)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(37808-903)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(37808-903) , pack(37808-903)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(37808-903)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.117025878manufacture(37808-903)

Revised: 8/2023
Document Id: 5c71c88d-abfe-448a-b049-6a6931b4c237
Set id: 9837e9af-c542-4c0f-be33-94927d67c6a7
Version: 7
Effective Time: 20230811
 
H E B