Label: MOTION SICKNESS RELIEF- meclizine hcl tablet
- NDC Code(s): 46122-535-51
- Packager: Amerisource Bergen
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- 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
- Directions
- Other information
- Inactive ingredients
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Principal display panel
GOOD
NEIGHBOR
PHARMACY®Compare to Dramamine® All Day Less Drowsy active ingredient*
NDC 46122-535-51
Motion Sickness Relief
meclizine HCl 25 mg / antiemeticLess Drowsy Formula
Helps prevent Nausea, Vomiting and Dizziness
due to Motion Sickness for up to 24 hoursAges 12 Years and Over
8 Tablets | 25 mg Each
Actual Size
TAMPER 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® Less Drowsy. 50844 ORG042340319Distributed By
AmerisourceBergen
1 West First Avenue
Conshohocken, PA 19428
Questions or Concerns?
www.mygnp.comGNP 44-403
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INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46122-535 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:46122-535-51 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 - Amerisource Bergen (007914906) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(46122-535) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(46122-535) , pack(46122-535) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(46122-535) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(46122-535)