NDC | 69842-403-21 |
Set ID | bb3a2d3e-8f5a-4e80-89bf-7291841995a5 |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS Pharmacy |
Generic Name | |
Product Class | Antiemetic |
Product Number | |
Application Number | PART336 |
- Active ingredient (in each tablet)
- Purpose
- Uses
-
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 or comments?
-
Principal display panel
CVS Health®
Compare to the active ingredient
in Dramamine® All Day Less Drowsy*All Day Protection
Motion Sickness
Less Drowsy FormulaMECLIZINE HYDROCHLORIDE TABLETS
AntiemeticPrevents up to 24 hours of
motion sickness•Protection with less drowsiness
•Prevents nausea, vomiting & dizziness
32 TABLETS (25 mg EACH)
Actual Size
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
*This product is not manufactured or distributed by Medtech Products Inc., owner of the registered trademark Dramamine® All Day Less Drowsy.
50844 ORG021940327
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
©2021 CVS/pharmacyCVS.com® 1-800-SHOP CVS
V-14236CVS®Quality
Money Back GuaranteeCVS 44-403
-
INGREDIENTS AND APPEARANCE
MOTION SICKNESS LESS DROWSY FORMULA
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-403 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 STARCH, CORN (UNII: O8232NY3SJ) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) MAGNESIUM STEARATE (UNII: 70097M6I30) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 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:69842-403-21 2 in 1 CARTON 06/24/2002 1 8 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:69842-403-27 4 in 1 CARTON 06/24/2002 2 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 - CVS Pharmacy (062312574) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 PACK(69842-403) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 MANUFACTURE(69842-403) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 PACK(69842-403)