Motion Sickness Relief

Product NDC: 41163-304
11-digit product format: 411630304
Labeler code: 41163
Product ID: 41163-304_cfee86fb-1d38-4c7f-be1f-d01752bf3f7a
Type: HUMAN OTC DRUG
Nonproprietary name: Meclizine HCl
Dosage form: TABLET
Route: ORAL
Labeler: United Natural Foods, Inc. dba UNFI
Application: M009
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2002-06-24
Substance: MECLIZINE HYDROCHLORIDE
Active strength: 25 mg/1
Pharmacologic classes: Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Motion Sickness Relief
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MECLIZINE HYDROCHLORIDE	25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
HDP7W44CIO	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
995666	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
108bb943-529f-4510-b770-b54eca493ae0	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ac6963c4-31c6-325f-ee58-83a0a06597ad	Product name	5	20221206

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41163-304-02	Motion Sickness Relief	12 in 1 BOTTLE, PLASTIC	TABLET	12		20
41163-304-02	Motion Sickness Relief	1 in 1 PACKAGE	TABLET	1		20

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
41163-304-02	EA - Each	41163-304	71b8f709-93e4-4c23-937e-9b718fe9d79b	1	2017-03-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MECLIZINE HYDROCHLORIDE	ACTIVE INGREDIENT	HDP7W44CIO	MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [SUPERVALU INC.]	6
MECLIZINE	ACTIVE MOIETY	3L5TQ84570	MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [SUPERVALU INC.]	6
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [SUPERVALU INC.]	6
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [SUPERVALU INC.]	6
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [SUPERVALU INC.]	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41163-304	MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [UNITED NATURAL FOODS, INC. DBA UNFI]	19	Current NDC, Legacy NDC, 2 package rows	20250122_108bb943-529f-4510-b770-b54eca493ae0.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 6 · 112 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dramamine Orange	DIMENHYDRINATE	Medtech Products Inc.	76166156-bce1-492f-833e-6bbd07859c3f	2026-09-17	Warnings	Exact identifier application number: M009
Pepto Nausea Motion Sickness	MECLIZINE HCL	THE PROCTER & GAMBLE MANUFACTURING COMPANY	29a1bd1e-d0e0-478f-e063-6394a90ab0aa	2026-09-10	Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	A-S Medication Solutions	2518b0b6-35ab-49f4-936c-1eafea04b466	2026-09-09	Warnings	Exact identifier application number: M009
Dramamine Less Drowsy	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	fa6a0969-7427-4b87-bc04-a2792665c218	2026-09-04	Warnings	Exact identifier application number: M009
Less Drowsy Motion Sickness Relief	MECLIZINE HCL	Wal-Mart Stores Inc	277a6266-e641-4621-bbb9-64195d51b66a	2026-08-28	Warnings	Exact identifier application number: M009
Nausea Relief	MECLIZINE HCL	WALMART INC.	8010741e-61b2-4c1f-9f0e-21612878fa0e	2026-08-28	Warnings	Exact identifier application number: M009
Motion Sickness	MECLIZINE HCL	H E B	9837e9af-c542-4c0f-be33-94927d67c6a7	2026-08-21	Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Bryant Ranch Prepack	cd82fca9-a8dc-4545-8e64-b67d644832e7	2026-08-20	Warnings	Exact identifier application number: M009
Motion Sickness	DIMENHYDRINATE	Strategic Sourcing Services LLC	be8f91d4-6e4f-4d47-93e9-7fb91160b7df	2026-08-17	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Walgreen Company	ace7eba4-e033-48f5-8533-c3ea9dfc32b0	2026-08-12	Warnings	Exact identifier application number: M009
Motion Sickness	MECLIZINE HCL	Strategic Sourcing Services LLC	76fb6471-09b0-4c51-bacc-b3533b6aa971	2026-08-07	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Cardinal Health 110, LLC. DBA Leader	ce83a868-bdd8-4c77-9bc0-664133028f75	2026-08-06	Warnings	Exact identifier application number: M009
Less Drowsy Formula Motion Sickness Relief	MECLIZINE HCL	Salado Sales, Inc.	273235b0-dacc-4a95-91be-91e13a2c6d10	2026-08-05	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	L.N.K. International, Inc.	8e1889de-fbef-44f1-bbfb-c68a78e6330c	2026-07-30	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Chain Drug Marketing Association, Inc.	00a327c6-6b86-4702-8c04-55c405c1404c	2026-07-23	Warnings	Exact identifier application number: M009
Pepto Motion Sickness	MECLIZINE HCL	THE PROCTER & GAMBLE MANUFACTURING COMPANY	571e3eeb-ae9e-7054-e063-6394a90a2634	2026-07-21	Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Rugby Laboratories	b57f14a7-3852-03db-e053-2a95a90a80d6	2026-07-16	Warnings	Exact identifier application number: M009
Motion Sickness	DIMENHYDRINATE	CVS Pharmacy	0998947c-cfba-497e-bf7a-9c7f8fff1764	2026-07-16	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Topco Associates, LLC	307e3144-3b01-4bd0-9155-6b58fc4cab92	2026-07-09	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	L.N.K. International, Inc.	95aae32f-6b3f-469d-86a5-c201a53f862a	2026-06-29	Warnings	Exact identifier application number: M009

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
HDP7W44CIO	MECLIZINE HYDROCHLORIDE	31884-77-2	MECLIZINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
995666	meclizine HCl 25 MG Oral Tablet	PSN	108bb943-529f-4510-b770-b54eca493ae0	20
995666	meclizine hydrochloride 25 MG Oral Tablet	SCD	108bb943-529f-4510-b770-b54eca493ae0	20

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
41163-304-02	41163030402	1 BOTTLE, PLASTIC in 1 PACKAGE (41163-304-02) / 12 TABLET in 1 BOTTLE, PLASTIC	2002-06-24	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Equaline 44-403	United Natural Foods, Inc. dba UNFI \| LNK International, Inc.	2026-01-12	HUMAN OTC DRUG LABEL	20