Meclizine 25mg by Innovida Pharmaeutique Corporation

Meclizine 25mg by

Drug Labeling and Warnings

Meclizine 25mg by is a Otc medication manufactured, distributed, or labeled by Innovida Pharmaeutique Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• prevents and treats nausea, vomiting or dizziness due to motion sickness

Warnings

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

Ask a doctor before use if you have

• glaucoma 
• a breathing problem such as emphysema or chronic bronchitis 
• trouble urinating due to an enlarged prostate gland

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

When using this product

• do not exceed recommended dosage 
• may cause drowsiness
• alcohol, sedatives, and tranquilizers may increase drowsiness 
• avoid alcoholic drinks 
• 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 ( 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

• Store in a dry place at 15°-30°C (59°-86°F) 
• keep lid tightly closed

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

MECLIZINE 25MG 
meclizine tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71800-052
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570)	MECLIZINE HYDROCHLORIDE	25 mg

Inactive Ingredients
Ingredient Name	Strength
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
Color	white (Off White)	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71800-052-03	1000 in 1 BOTTLE; Type 0: Not a Combination Product	02/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	02/10/2025	12/31/2025

Labeler - Innovida Pharmaeutique Corporation (080892908)

Revised: 12/2025

Document Id: 46e11bc1-bb76-9eca-e063-6394a90a4288

34390-5

Set id: 5e49ee86-ced5-4ef0-9354-08478320a1a9

Version: 2

Effective Time: 20251226