Label: MECLIZINE HCL- meclizine hydrochloride chewable tablet, chewable
- NDC Code(s): 16571-824-01, 16571-824-10
- Packager: Rising Pharma Holdings, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 8, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts Active ingredient (in each chewable tablet)
- Purpose
- Uses
- Warnings
- ASK DOCTOR/PHARMACIST
- When using this product
- PREGNANCY OR BREAST FEEDING
- Keep out of reach of children.
- Directions
- Other Information
- Inactive ingredients
- Questions or comments?
- TAMPER EVIDENT: DO NOT USE IF FOIL SEAL UNDER CAP, PRINTED WITH"SEALED for YOUR PROTECTION" IS BROKEN OR MISSING.Rising Pharma Holdings, Inc. is not affiliated with the owner of the registered trademark Bonine® Manufactured by: Unique Pharmaceutical Laboratories(A Div. of J.B. Chemicals & Pharmaceuticals Ltd.),Mumbai 400 030, India Distributed by: Rising Pharma Holdings, Inc.East Brunswick, NJ 08816 Mfg. Lic. No.: G/1430Feb 2022
- PRINCIPAL DISPLAY PANEL - 25 mg Chewable Tablet Label
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INGREDIENTS AND APPEARANCE
MECLIZINE HCL
meclizine hydrochloride chewable tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:16571-824 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 ASPARTAME (UNII: Z0H242BBR1) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DEXTROSE (UNII: IY9XDZ35W2) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) RASPBERRY (UNII: 4N14V5R27W) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) SUCROSE (UNII: C151H8M554) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) Product Characteristics Color pink (Pink to light pink) Score 2 pieces Shape ROUND Size 8mm Flavor RASPBERRY Imprint Code M Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:16571-824-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 08/18/2022 2 NDC:16571-824-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 08/18/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M009.50 08/18/2022 Labeler - Rising Pharma Holdings, Inc. (116880195) Registrant - Unique Pharmaceutical Laboratories (917165052) Establishment Name Address ID/FEI Business Operations Unique Pharmaceutical Laboratories 650434645 manufacture(16571-824)