Label: NAUSEA RELIEF- meclizine hcl tablet
- NDC Code(s): 79903-177-10
- Packager: WALMART INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 28, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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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?
-
Principal display panel
equate™
NDC 79903-177-10
Compare to
Dramamine®
Nausea active
ingredient*Nausea Relief
Meclizine HCl 25 mgAntiemetic
• Relieves Motion-Related
Nausea, dizziness
& vomitingFor Ages 12 Years and Over
UP TO
24
HOURSActual Size
10
TABLETSTAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERINGSatisfaction guaranteed - Or we'll replace it or give you your money back. For
questions or comments please call 1-888-287-1915.DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
PRODUCT OF INDIA
*This product is not manufactured or distributed by Medtech Products Inc.,
owner of the registered trademark Dramamine® Nausea. 50844 ORG042340303Equate 44-403N
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INGREDIENTS AND APPEARANCE
NAUSEA RELIEF
meclizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-177 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:79903-177-10 2 in 1 CARTON 05/16/2023 1 5 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 05/16/2023 Labeler - WALMART INC. (051957769) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(79903-177) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(79903-177) , pack(79903-177) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(79903-177) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(79903-177)