Label: MOTION SICKNESS RELIEF- meclizine hcl tablet
- NDC Code(s): 50844-403-19
- Packager: L.N.K. International, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 7, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- difficulty in urination due to enlargement of the prostate gland
- glaucoma
- a breathing problem such as emphysema or chronic bronchitis
- difficulty in urination due to enlargement of the prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
QUALITY
+PLUSNDC 50844-403-19
*Compare to active ingredient in
Dramamine® Less DrowsyMotion Sickness
Relief
LESS DROWSY FORMULA
Meclizine HCl 25 mg • AntiemeticHELPS PREVENT NAUSEA, VOMITING AND
DIZZINESS DUE TO MOTION SICKNESS
FOR UP TO 24 HOURSAges 12 Years and Over
8Tablets
ACTUAL
SIZETAMPER EVIDENT: DO NOT USE IF
PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS
ANY SIGNS OF TAMPERING*This product is not manufactured or distributed by Medtech Products Inc., owner of the registered trademark
Dramamine® All Day Less Drowsy. 50844 ORG042340319Distributed by
LNK INTERNATIONAL, INC.
60 Arkay Drive
Hauppauge, NY 11788
USAQuality Plus 44-403A
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INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50844-403 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 SILICON DIOXIDE (UNII: ETJ7Z6XBU4) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) STARCH, CORN (UNII: O8232NY3SJ) 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:50844-403-19 1 in 1 CARTON 06/24/2002 1 8 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 Drug M009 06/24/2002 Labeler - L.N.K. International, Inc. (038154464) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(50844-403) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(50844-403) , pack(50844-403) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(50844-403) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(50844-403)