WAL-DRAM 2 QUICK-DISSOLVING- meclizine hydrochloride tablet, orally disintegrating

Wal-Dram 2 Quick-Dissolving by

Drug Labeling and Warnings

Wal-Dram 2 Quick-Dissolving by is a Otc medication manufactured, distributed, or labeled by Walgreen Co., Sato Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient (in each tablet) 
Meclizine hydrochloride 25mg

PURPOSE

Purpose
Meclizine hydrochloride    Antiemetic

Uses for the prevention and treatment of the nausea, vomiting, or dizziness associated with motion sickness

WARNINGS

​Warnings

Do not use in children under 12 years of age unless directed by a physician

Ask a doctor before use if you have
■ glaucoma   ■ a breathing problem such as emphysema or chronic bronchitis
■ difficulty in urination due to enlargement of the prostate gland

Ask a physician or pharmacist before use if you are
■ taking sedatives or tranquilizers

When using this product
■ you may get drowsy   ■ avoid alcoholic beverages
■ be careful when driving a motor vehicle or operating machinery
■ alcohol, sedatives, and tranquilizers may increase the drowsiness effect

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.

DOSAGE & ADMINISTRATION

Directions
to prevent motion sickness take it at least one hour before traveling    
adults and children 12 years of age and over:  take 1 to 2 (25 to 50 mg) tablets once daily, or as directed by a physician.

OTHER SAFETY INFORMATION

Other information
■ store at 20-30°C (68-86°F)

INACTIVE INGREDIENT

Inactive ingredients
acesulfame potassium, erythritol, hydroxypropyl cellulose, colloidal silicon dioxide, mannitol, menthol, sodium stearyl fumarate, yellow ferric oxide.

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WAL-DRAM 2 QUICK-DISSOLVING 
meclizine hydrochloride tablet, orally disintegrating

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1407
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
ERYTHRITOL (UNII: RA96B954X6)
MANNITOL (UNII: 3OWL53L36A)
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
silicon dioxide (UNII: ETJ7Z6XBU4)
LEVOMENTHOL (UNII: BZ1R15MTK7)

Product Characteristics
Color	yellow	Score	no score
Shape	ROUND	Size	13mm
Flavor		Imprint Code	SJ
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1407-01	2 in 1 CARTON	03/01/2016
1		6 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 0363-1407-02	3 in 1 CARTON	10/23/2018
2		6 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part336	03/01/2016

Labeler - Walgreen Co. (008965063)

Registrant - Sato Pharmaceutical Co., Ltd. (690575642)