Label: WAL DRAM- meclizine hcl tablet
- NDC Code(s): 0363-0403-21
- Packager: Walgreen Company
- 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.
Drug Label Information
Updated March 30, 2021
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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
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- Directions
- Other information
- Inactive ingredients
- Questions of comments?
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Principal Display Panel
Walgreens
Compare to Dramamine® All Day Less Drowsy active ingredient††
NDC 0363-0403-21
Wal-Dram® 2
MECLIZINE HCl TABLETS, 25 mg / ANTIEMETICALL DAY RELIEF LESS DROWSY FORMULA
• Helps prevent nausea & dizziness
due to motion sickness
• All-day relief of motion sickness16 TABLETS
Actual Size
†Walgreens Pharmacist Survey
††This product is not manufactured or distributed by Medtech Products Inc., owner of the registered trademark Dramamine® All Day Less Drowsy.50844 REV0219B40321
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
Walgreens 44-403
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INGREDIENTS AND APPEARANCE
WAL DRAM
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0403 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 D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) MAGNESIUM STEARATE (UNII: 70097M6I30) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) Product Characteristics Color yellow Score no score Shape ROUND Size 9mm Flavor Imprint Code 44;403 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0403-21 2 in 1 CARTON 06/24/2002 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 final part336 06/24/2002 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(0363-0403) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(0363-0403) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 pack(0363-0403)