MECLIZINE 25MG- meclizine tablet, chewable 
Innovida Pharmaeutique Corporation

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Active Ingredient (in each chewable tablet)

Meclizine HCl 25 mg

Purpose

Expectorant

Uses

Warnings

Do not usein children under 12 years of age unless directed by a doctor

Ask a doctor before use if you have

Ask a doctor or pharmacist before use ifyou are taking sedatives or tranquilizers

When using this product

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 ( 1-800-222-1222).

Directions

Dosage should be taken one hour before travel starts

 adults and children 12 years of age and over chew 1 to 2 tablets once daily, or as directed by a doctor
 children under 12 years of age do not give this product to children under 12 years of age unless directed
by a doctor

Other Information

Inactive Ingredients

Croscarmellose Sodium, Crospovidone, FD&C Red #40 Lake, French Vanilla Flavor, Lactose, Magnesium Stearate, Raspberry Flavor, Silica,
Sodium Saccharin, Stearic Acid

Questions or Comments? 1-888-462-4166

Product label

image description

MECLIZINE 25MG 
meclizine tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71800-052
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
CROSPOVIDONE (UNII: 2S7830E561)  
VANILLA (UNII: Q74T35078H)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
RASPBERRY (UNII: 4N14V5R27W)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
Product Characteristics
Colorwhite (Off White) Scoreno score
ShapeROUNDSize9mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71800-052-031000 in 1 BOTTLE; Type 0: Not a Combination Product02/10/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01202/10/2025
Labeler - Innovida Pharmaeutique Corporation (080892908)

Revised: 2/2025
Document Id: 2f25a39e-240e-5ea9-e063-6294a90a3ab2
Set id: 5e49ee86-ced5-4ef0-9354-08478320a1a9
Version: 1
Effective Time: 20250227
 
Innovida Pharmaeutique Corporation