Label: BONINE MAX- meclizine hydrochloride tablet, chewable
- NDC Code(s): 65197-520-16
- Packager: WellSpring Pharmaceutical Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 5, 2022
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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
- Directions
- Other information
- Inactive ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
NDC 65197-520-16
BONINE MAX STRENGTH
Prevents and treats: Dizziness - Nausea - Vomiting - Motion sickness
** Results may vary
ATTENTION: DO NOT USE IF CARTON IS OPEN OR IF BLISTER IS TORN OR MISSING. Keep carton for important drug facts information.
MONEY BACK GUARANTEED
Dist. by: WellSpring Pharmaceutical Corporation
Sarasota, FL 34243 USA© 2023 WellSpring Pharmaceutical Corporation
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BONINE MAX
meclizine hydrochloride tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65197-520 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE 50 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) STARCH, CORN (UNII: O8232NY3SJ) PEPPERMINT (UNII: V95R5KMY2B) FD&C RED NO. 40 (UNII: WZB9127XOA) SACCHARIN SODIUM (UNII: SB8ZUX40TY) MAGNESIUM STEARATE (UNII: 70097M6I30) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color white Score no score Shape ROUND Size 8mm Flavor PEPPERMINT Imprint Code BMX Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65197-520-16 2 in 1 BOX 03/24/2023 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 03/24/2023 Labeler - WellSpring Pharmaceutical Corporation (110999054)