Label: CVS MOTION SICKNESS FAST MELTING- meclizine hydrochloride tablet, orally disintegrating
- NDC Code(s): 59779-534-01
- Packager: CVS Pharmacy, Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Updated August 27, 2015
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- ACTIVE INGREDIENT
Active ingredient (in each tablet)Close
Meclizine hydrochloride 25mg
Meclizine hydrochloride Antiemetic
- INDICATIONS & USAGE
■ For the prevention and treatment of the nausea, vomiting, or dizziness associated with motion sickness.
Ask a doctor before use if you have
■ glaucoma ■ a breathing problem such as emphysema or chronic bronchitis
■ difficulty in urination due to enlargement of the prostate gland
When using this product
■ you may get drowsy ■ avoid alcoholic beverages
■ be careful when driving a motor vehicle or operating machinery
■ alcohol, sedatives, and tranquilizers may increase the drowsiness effect
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
- DOSAGE & ADMINISTRATION
To prevent motion sickness take it at least one hour before traveling
Adults and children 12 years of age and over: take 1 to 2 (25 to 50 mg) tablets once daily, or as directed by a physician.
- OTHER SAFETY INFORMATION
■ Store at 20-30°C (68-86°F)
- INACTIVE INGREDIENT
acesulfame potassium, erythritol, hydroxypropyl cellulose, colloidal silicon dioxide, mannitol, menthol, sodium stearyl fumarate, yellow ferric oxide.
- INGREDIENTS AND APPEARANCE
CVS MOTION SICKNESS FAST MELTING
meclizine hydrochloride tablet, orally disintegrating
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-534 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 ERYTHRITOL (UNII: RA96B954X6) MANNITOL (UNII: 3OWL53L36A) ACESULFAME POTASSIUM (UNII: 23OV73Q5G9) HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI) COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) LEVOMENTHOL (UNII: BZ1R15MTK7) Product Characteristics Color yellow Score no score Shape ROUND Size 13mm Flavor Imprint Code SJ Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-534-01 1 in 1 CARTON 1 12 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 final part336 08/27/2015 Labeler - CVS Pharmacy, Inc. (062312574)