MOTION SICKNESS RELIEF- meclizine hcl tablet 
United Natural Foods, Inc. dba UNFI

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Equaline 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

  • glaucoma
  • difficulty in urination due to enlargement of the prostate gland
  • 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?

1-855-423-2630

Principal Display Panel

EQUALINE®

compare to Dramamine®
Less Drowsy

active ingredient*
NDC 41163-304-02

motion sickness relief
meclizine HCl 25 mg
(antiemetic)

less drowsy formula

Ages 12 Years & Over
helps prevent nausea & dizziness
due to motion sickness
for up to 24 hours

12 tablets 

TAMPER EVIDENT:
USE ONLY IF THIS BLISTER IS INTACT

actual size

*This product is not manufactured or distributed by
Medtech Products Inc., owner of the registered
trademark Dramamine® Less Drowsy.
50844 ORG042340302

100% Quality
GUARANTEED

DISTRIBUTED BY UNFI
PROVIDENCE, RI 02908 USA
855-423-2630

Equaline 44-403

Equaline 44-403

MOTION SICKNESS RELIEF 
meclizine hcl tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-304
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:41163-304-021 in 1 PACKAGE06/24/2002
112 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00906/24/2002
Labeler - United Natural Foods, Inc. dba UNFI (943556183)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(41163-304)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(41163-304) , pack(41163-304)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(41163-304)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.117025878manufacture(41163-304)

Revised: 1/2024
Document Id: 1ec80c6f-5f59-48fb-95c1-91b043117e72
Set id: 108bb943-529f-4510-b770-b54eca493ae0
Version: 18
Effective Time: 20240116
 
United Natural Foods, Inc. dba UNFI