Label: WAL-DRAM 2 QUICK-DISSOLVING- meclizine hydrochloride tablet, orally disintegrating
- NDC Code(s): 0363-1407-01, 0363-1407-02
- Packager: Walgreen Co.
- 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 December 30, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Uses • for the prevention and treatment of the nausea, vomiting, or dizziness associated with motion sickness
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WARNINGS
Warnings
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 - DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- Carton Image -01
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INGREDIENTS AND APPEARANCE
WAL-DRAM 2 QUICK-DISSOLVING
meclizine hydrochloride tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1407 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 (1600000 WAMW) (UNII: RFW2ET671P) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI) 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:0363-1407-01 2 in 1 CARTON 03/01/2016 1 6 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0363-1407-02 3 in 1 CARTON 10/23/2018 2 6 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 03/01/2016 Labeler - Walgreen Co. (008965063) Registrant - Sato Pharmaceutical Co., Ltd. (690575642)