Label: MOTION SICKNESS RELIEF- meclizine hcl tablet
- NDC Code(s): 55319-903-19
- Packager: Family Dollar Services Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 2, 2024
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- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
Ask a doctor before use if you have
- difficulty in urination due to enlargement of the prostate gland
- glaucoma
- a breathing problem such as emphysema or chronic bronchitis
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal display panel
FAMILY
Wellness™COMPARE TO THE ACTIVE
INGREDIENT IN DRAMAMINE®
LESS DROWSY*LESS DROWSY FORMULA
MOTION SICKNESS
RELIEF
Meclizine HCl 25 mg
AntiemeticHelps prevent nausea, vomiting
and dizziness due to motion sickness
for up to 24 hoursAges 12 Years and Over
8 TABLETS
24
HOURACTUAL SIZE
NDC 55319-903-19
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® Less Drowsy.
50844 ORG042340319DISTRIBUTED BY: MIDWOOD BRANDS LLC,
500 VOLVO PKWY, CHESAPEAKE, VA 23320 USANOT 100% SATISFIED?
Return within 30 days to the
store of purchase for a refund
(with receipt) or exchange.Family Wellness 44-403A
-
INGREDIENTS AND APPEARANCE
MOTION SICKNESS RELIEF
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55319-903 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 SILICON DIOXIDE (UNII: ETJ7Z6XBU4) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) STARCH, CORN (UNII: O8232NY3SJ) 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:55319-903-19 1 in 1 CARTON 12/29/2023 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 Drug M009 12/29/2023 Labeler - Family Dollar Services Inc (024472631) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(55319-903) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(55319-903) , pack(55319-903) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(55319-903) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(55319-903)