Label: MOTION SICKNESS RELIEF- meclizine hcl tablet
- NDC Code(s): 30142-943-19
- Packager: Kroger Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 9, 2023
If you are a consumer or patient please visit this version.
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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
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
COMPARE TO the active ingredient in DRAMAMINE®
LESS DROWSY FORMULA *See side panelNDC 30142-943-19
Kroger®
Up to 24 Hours of Relief
Motion Sickness Relief
Meclizine HCl 25 mg, Antiemetic
Less Drowsy FormulaHelps Prevent Nausea & Dizziness
Due to Motion Sickness
Ages 12 Years and Over8 TABLETS
actual size
OPEN HERE TO
VIEW COMPLETE
PRODUCT INFORMATIONTAMPER EVIDENT: DO NOT USE IF
PRINTED TEAR STRIP IS BROKEN
OR MISSING
*This product is not manufactured or distributed by Medtech Products Inc.,
owner of the registered trademark Dramamine® Less Drowsy Formula.
50844 ORG021940319DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OHIO 45202QUALITY GUARANTEE
800-632-6900 | www.kroger.comKroger 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:30142-943 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:30142-943-19 8 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/03/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M009 06/03/2019 Labeler - Kroger Company (006999528) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(30142-943) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(30142-943) , pack(30142-943) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(30142-943) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(30142-943)