Label: MOTION SICKNESS RELIEF- meclizine hydrochloride tablet, chewable
- NDC Code(s): 41163-404-21
- Packager: SUPERVALU INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- Active ingredient (in each tablet)
Meclizine HCl 25 mgClose
- prevents and treats nausea, vomiting, or dizzines associated with motion sickness
Ask a doctor before use if you have
- difficulty in urination due to enlargement of the prostate gland
- a breathing problem such as emphysema or chronic bronchitis
When using this product
- do not exceed recommended dosage
- drowsiness may occur
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careul when driving a motor vehicle or operating machinery
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center rigth away.
- dosage should be taken one hour before travel starts
- adults and children 12 years of age and over: take 1 to 2 tablets once daily or as directed by a doctor
- Other information
- store at controlled room temperature 15º-30ºC (59º-86ºF)
- protect from heat and humidity
- for better identification keep talbets in carton until used
- see end flap for expiration date and lot number
- Inactive ingredients
corn starch, FD&C red #40 aluminum lake, lactose, magnesium stearate, rasberry flavor, silica gel, sodium saccharinClose
- Questions or comments?
- Principal Display Panel
compare to Bonine® tablets active ingredients*
meclizine HCl 25 mg • antiemetic
• prevents motion sickness
• causes less drowsiness
16 chewable tablets
*This product is not manufactured or distributed by Insight Pharmaceuticals, owner of the registered trademark Bonine® Chewable Tablets.
DISTRIBUTED BY SUPERVALU INC.
EDEN PRARIE, MN 55344 USA
TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
- INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
meclizine hcl tablet, chewable
Product Information Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:41163-404 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MECLIZINE HYDROCHLORIDE (MECLIZINE) MECLIZINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 LACTOSE MAGNESIUM STEARATE Product Characteristics Color PINK Score no score Shape ROUND Size 10mm Flavor RASPBERRY Imprint Code 44;404 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41163-404-21 1 in 1 CARTON 1 16 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part336 05/29/2002 Labeler - SUPERVALU INC. (006961411) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 PACK(41163-404) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 MANUFACTURE(41163-404)