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Motion Sickness Relief by L.N.K. International, Inc.

Dosage form: tablet
Ingredients: DIMENHYDRINATE 50mg
Labeler: L.N.K. International, Inc.
NDC Code: 50844-199

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Quality Plus 44-198

Active ingredient (in each tablet)

Dimenhydrinate 50 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 2 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 urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product
  • marked 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, the first dose should be taken one-half to one hour before starting activity
adults and
children 12
years and over
1 to 2 tablets every 4-6 hours; do not exceed
8 tablets in 24 hours, or as directed by a
doctor.
children 6 to 
under 12 years
1/2 to 1 tablet every 6-8 hours; do not exceed
3 tablets in 24 hours, or as directed by a 
doctor
children 2 to
under 6 years
1/2 tablet every 6-8 hours, do not exceed 1 1/2
tablets in 24 hours, 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 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF) 
  • protect from moisture
  • see end flap for expiration date and lot number

Inactive ingredients

croscarmellose sodium, dicalcium phosphate, magnesium stearate, microcrystalline cellulose, silica gel, stearic acid

Questions or comments?

1-800-426-9391

Principal display panel

QUALITY
    +PLUS

NDC 50844-199-02

*Compare to active ingredient in
  Dramamine® Original Formula

ORIGINAL FORMULA

Motion Sickness Relief
Dimenhydrinate 50 mg •  Antiemetic

FAST ACTING RELIEF
OF MOTION SICKNESS FOR
CHILDREN & ADULTS

12 Tablets

ACTUAL SIZE

*This product is not manufactured or distributed by Prestige Brands, Inc., owner
of the registered trademark Dramamine® Original Formula.

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

Distributed by
LNK INTERNATIONAL, INC.
60 Arkay Drive
Hauppauge, NY 11788 USA

50844    ORG111519802

Quality Plus 44-198

MOTION SICKNESS RELIEF 
dimenhydrinate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50844-199
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMENHYDRINATE (DIPHENHYDRAMINE and CHLORTHEOPHYLLINE) DIMENHYDRINATE50 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM 
MAGNESIUM STEARATE 
MICROCRYSTALLINE CELLULOSE 
SILICON DIOXIDE 
STEARIC ACID 
ANHYDROUS DIBASIC CALCIUM PHOSPHATE 
Product Characteristics
ColorWHITEScore2 pieces
ShapeROUNDSize9mm
FlavorImprint Code44;198
Contains    
Packaging
#Item CodePackage Description
1NDC:50844-199-022 BLISTER PACK in 1 CARTON
16 TABLET in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33612/01/1992
Labeler - L.N.K. International, Inc. (038154464)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(50844-199)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(50844-199)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(50844-199)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088PACK(50844-199)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(50844-199)

 
L.N.K. International, Inc.

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Medically reviewed on Nov 7, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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