OTC Medication Information: Motion Sickness Relief

MOTION SICKNESS RELIEF- meclizine hydrochloride tablet
DOLGENCORP, LLC

Active ingredient (in each tablet)

Meclizine HCl 25 mg

Purpose

Antiemetic

Uses

for the prevention and treatment of 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

  • glaucoma

  • difficulty in urination due to enlargement of the prostate gland

  • a breathing problem such as emphysema or chronic bronchitis

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

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

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 (1-800-222-1222) right away.

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 over: 1 to 2 tablets once daily, or as directed by a doctor

Other information

  • TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN

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

  • protect from heat and humidity

  • see end flap for expiration date and lot number

Inactive ingredients

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

Questions or comments?

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Compare to the
active ingredient of
Dramamine® All Day
Less Drowsy*

Less Drowsy Formula
Motion Sickness
Relief

Meclizine HCl 25 mg / Antiemetic

• Up to 24 hours of protection
• Prevents nausea , dizziness & vomiting

8 Tablets

Actual Tablet Size

25
mg each

TAMPER EVIDENT: DO NOT USE IF
PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS
ANY SIGNS OF TAMPERING

DISTRIBUTED BY
DOLGENCORP, LLC
100 MISSION RIDGE
GOODLETTSVILLE, TN 37072

100%
Satisfaction
Guaranteed
(888)-309-9030

*This product is not manufactured or distributed by
Medtech Products Inc., owner of the registered trademark
Dramamine® All Day Less Drowsy.50844 ORG021940319

Dollar General 44-403
(click image for full-size original)

Dollar General 44-403

MOTION SICKNESS RELIEF meclizine hcl tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-943
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE (MECLIZINE) MECLIZINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
D&C YELLOW NO. 10 ALUMINUM LAKE
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
SILICON DIOXIDE
Product Characteristics
Color yellow Score no score
Shape ROUND Size 9mm
Flavor Imprint Code 44;403
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:55910-943-19 1 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 8 TABLET in 1 BLISTER PACK This package is contained within the CARTON (55910-943-19)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M009 06/01/2019
Labeler — DOLGENCORP, LLC (068331990)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 038154464 pack (55910-943)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 832867837 manufacture (55910-943), pack (55910-943)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 967626305 pack (55910-943)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 117025878 manufacture (55910-943)

Revised: 04/2023 DOLGENCORP, LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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