Nausea Relief

Product NDC
79903-177
11-digit product format
799030177
Labeler code
79903
Product ID
79903-177_c0e5efd6-39a2-4775-b4da-e1a3b24084ea
Type
HUMAN OTC DRUG
Nonproprietary name
Meclizine HCl
Dosage form
TABLET
Route
ORAL
Labeler
WALMART INC.
Application
M009
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-05-16
Substance
MECLIZINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Nausea Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MECLIZINE HYDROCHLORIDE25 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiHDP7W44CIO
Rxcui995666

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ac6963c4-31c6-325f-ee58-83a0a06597adProduct name520221206

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-177-10Nausea Relief2 in 1 CARTONTABLET25
79903-177-10Nausea Relief5 in 1 BLISTER PACKTABLET55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-177NAUSEA RELIEF (MECLIZINE HCL) TABLET [WALMART INC.]4Current NDC, 2 package rows20240825_8010741e-61b2-4c1f-9f0e-21612878fa0e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
995666meclizine HCl 25 MG Oral TabletPSN8010741e-61b2-4c1f-9f0e-21612878fa0e5
995666meclizine hydrochloride 25 MG Oral TabletSCD8010741e-61b2-4c1f-9f0e-21612878fa0e5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79903-177-10799030177102 BLISTER PACK in 1 CARTON (79903-177-10) / 5 TABLET in 1 BLISTER PACK2 blister pack2023-05-16NoNoHistorical