Label: MECLIZINE HCL- meclizine hydrochloride chewable tablet, chewable
- NDC Code(s): 68001-529-00, 68001-529-08
- Packager: BluePoint Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 14, 2022
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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?
- 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:68001-529 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) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) SUCROSE (UNII: C151H8M554) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DEXTROSE (UNII: IY9XDZ35W2) MALTODEXTRIN (UNII: 7CVR7L4A2D) RASPBERRY (UNII: 4N14V5R27W) 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:68001-529-00 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2022 2 NDC:68001-529-08 1000 in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part336 03/14/2022 Labeler - BluePoint Laboratories (985523874) Registrant - Unique Pharmaceutical Laboratories (917165052) Establishment Name Address ID/FEI Business Operations Unique Pharmaceutical Laboratories 650434645 manufacture(68001-529)