MEDIQUE MEDI-MECLIZINE- meclizine hcl tablet

Medique Medi-Meclizine by

Drug Labeling and Warnings

Medique Medi-Meclizine by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient (in each tablet)

Meclizine Hydrochloride 25 mg

PURPOSE

Purpose

Antiemetic

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

DO NOT USE

Do not use for children under 12 years of age unless directed by a doctor.

ASK DOCTOR

Ask a doctor before use if you have

■ difficulty in urination due to enlargement of the prostate gland

■ glaucoma

■ a breathing problems such as emphysema or chronic bronchitis

ASK DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

WHEN USING

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

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center
(1-800-222-1222) right away.

DOSAGE & ADMINISTRATION

Directions

■ to prevent motion sickness, take the first dose ½ hour to 1 hour before starting activity

■ to treat motion sickness, take at first signs of symptoms

Adults and children: (12 years and older) 1 to 2 tablets once daily, or as directed by a doctor.

Children under 12 years: Do not give to children under 12 years of age.

OTHER SAFETY INFORMATION

Other information

■ tamper-evident sealed packets

■ do not use any opened or torn packets

■ store at 77°F (25°C); excursions permitted between 59- 86º F (15-30ºC)

■ protect from heat and humidity

■ use by expiration date on packet

INACTIVE INGREDIENT

Inactive ingredients

corn starch, D&C yellow # 10 aluminum lake, lactose anhydrous, magnesium stearate, silicon dioxide

QUESTIONS

Questions or comments? Call 1-800-634-7680

Medique Medi-Meclizine Label

Medique®

Medi-Meclizine

All Day Relief

Alivio que Perdura Todo el Dia

Pull to Open

Tire Para Abrir

For the Prevention and Treatment of Motion Sickness Meclizine HCl 25mg

Para la Prevencion y el Tratamiento del Mareo “Mal del Viajero” Hidrochloruro de Meclizina 25mg

100 Tablets

(50 x 2)

Tamper Evident Unit Dose Packets

Empaquetado con Sellado Evidente en Dosis Unitarias

INGREDIENTS AND APPEARANCE

MEDIQUE MEDI-MECLIZINE 
meclizine hcl tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-481
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
STARCH, CORN (UNII: O8232NY3SJ)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
MAGNESIUM STEARATE (UNII: 70097M6I30)
D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)

Product Characteristics
Color	yellow	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	44;403
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-481-99	2 in 1 PACKET; Type 0: Not a Combination Product	12/14/2020
2	NDC: 47682-481-15	500 in 1 BOX	12/14/2020
2		2 in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 47682-481-33	50 in 1 BOX	12/14/2020
3		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M009	12/14/2020

Labeler - Unifirst First Aid Corporation (832947092)