Drug Facts

Active ingredient (in each tablet)

Meclizine HCI 25 mg

Purpose

Antiemetic

Uses

prevents and treats 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

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

Ask a doctor or pharmacist before use if you are

taking

sedatives
tranquilizers

When using this product

drowsiness may occur
alcohol, sedatives, and tranquilizers may increase drowsiness
avoid alcoholic drinks
be careful when driving a motor vehicle or operating machinery

If pregnant or breast-feeding,

ask a doctor before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center.

Directions

take first dose one hour before starting activity
adults and children 12 years and over: 1 to 2 tablets once daily, or as directed by a doctor

Inactive ingredients

calcium stearate, FD&C red #40 aluminum lake, lactose, microcrystalline cellulose, silicon dioxide, Sodium starch glycolate

Other Information

store at room temperature between 59º - 86ºF (15 - 30ºC)
protect from excessive moisture.

PRINCIPAL DISPLAY PANEL

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less drowsy

motion sickness relief tabs

Meclizine Hydrochloride

antiemetic

provides Up To 24 Hours of Motion Sickness Protection

prevents nausea, dizziness, vomiting

8 TABLETS (25 mg EACH) new smaller size

Retain carton for complete product information.

Distributed by: Drug Mart-Food Fair

211 Commerce Dr., Medina, Ohio 44256

Questions?: 866-467-2748

carton

label

LESS DROWSY MOTION SICKNESS RELIEF
meclizine hydrochloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:53943-826
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
FD&C RED NO. 40 (UNII: WZB9127XOA)
CALCIUM STEARATE (UNII: 776XM7047L)
LACTOSE (UNII: J2B2A4N98G)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)

Product Characteristics
Color	pink	Score	no score
Shape	ROUND	Size	7mm
Flavor		Imprint Code	25
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:53943-826-29	8 in 1 BLISTER PACK	12/01/2014
1		1 in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M009	12/01/2014

Labeler - Discount Drug Mart (047741335)

Name	Address	ID/FEI	Business Operations
Establishment
Bell Pharmaceuticals, Inc.		140653770	manufacture(53943-826)