Motion Sickness Relief

Product NDC: 49035-981
11-digit product format: 490350981
Labeler code: 49035
Product ID: 49035-981_f396818a-fa5a-43b1-b45d-b7849230db6a
Type: HUMAN OTC DRUG
Nonproprietary name: Dimenhydrinate
Dosage form: TABLET
Route: ORAL
Labeler: Wal-Mart Stores Inc
Application: M009
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1992-12-01
Substance: DIMENHYDRINATE
Active strength: 50 mg/1
Pharmacologic classes: Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
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
DIMENHYDRINATE	50 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
JB937PER5C	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198603	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
c25a7f2b-0f01-4ec0-8849-f08c23608d1d	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49035-981-12	Motion Sickness Relief	100 in 1 BOTTLE, PLASTIC	TABLET	100		16

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49035-981-12	EA - Each	49035-981	8954823d-b905-4814-b59f-ed6ce1f91b35	1	2024-04-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIMENHYDRINATE	ACTIVE INGREDIENT	JB937PER5C	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	3
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	3
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	L11K75P92J	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	3
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	3
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-981	MOTION SICKNESS RELIEF (DIMENHYDRINATE) TABLET [WAL-MART STORES INC]	15	Current NDC, Legacy NDC, 1 package rows	20250217_c25a7f2b-0f01-4ec0-8849-f08c23608d1d.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 3 of 6 · 107 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	NuCare Pharmaceuticals,Inc.	d0d8b376-8fe9-8776-e053-2a95a90ae651	2026-01-27	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	4f806804-48c7-414e-a177-5d3daf5b22e3	2026-01-20	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	United Natural Foods, Inc. dba UNFI	108bb943-529f-4510-b770-b54eca493ae0	2026-01-12	Warnings	Exact identifier application number: M009
Less Drowsy Motion Sickness Relief	MECLIZINE HCL	Rite Aid Corporation	2f9ebe6b-ffde-41de-9eaa-b03d87d33005	2026-01-09	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Rite Aid Corporation	4f532984-aeee-4dde-972c-742bdf12868f	2026-01-07	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Family Dollar Services Inc	e34126e3-52ef-4999-bf61-cba9b1818259	2026-01-05	Warnings	Exact identifier application number: M009
CVS Motion Sickness Fast Melting	MECLIZINE HYDROCHLORIDE	CVS Pharmacy, Inc.	2a723bce-a581-4558-b028-22f1f9125dd5	2025-12-30	Warnings	Exact identifier application number: M009
Wal-Dram 2 Quick-Dissolving	MECLIZINE HYDROCHLORIDE	Walgreen Co.	f3116203-1b8f-438a-b779-7bdd90eaf79e	2025-12-30	Warnings	Exact identifier application number: M009
MECLIZINE	MECLIZINE HCL 12.5 MG	Pharbest Pharmaceuticals, Inc.	8b3c9283-b618-4d57-9f15-7cf73e8737f5	2025-12-24	Warnings	Exact identifier application number: M009
MECLIZINE	MECLIZINE HCL 25MG	Pharbest Pharmaceuticals, Inc.	4bac2765-045c-405e-8006-8c5cfdfa89bc	2025-12-24	Warnings	Exact identifier application number: M009
DRAMAMINE	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	fdcbcc4e-9370-4975-8905-1f12c73fdc8c	2025-12-23	Warnings	Exact identifier application number: M009
DRAMAMINE	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	3a960d43-62aa-464e-92b9-d83042ba02bf	2025-12-23	Warnings	Exact identifier application number: M009
DRAMAMINE	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	6efd3473-ee14-4ee0-8a58-d15a64a9224a	2025-12-18	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Rite Aid Corporation	e599dc64-ac10-4f4e-9318-e9fab0526488	2025-11-15	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Kroger Company	64e0496c-5e09-46e9-94b9-624163d71b60	2025-11-05	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Walgreen Company	27bd9c74-c85e-4eeb-9e43-4120f9001187	2025-11-05	Warnings	Exact identifier application number: M009
Dramamine Original Formula	DIMENHYDRINATE	Medtech Products Inc.	f9302a5a-295a-4501-9332-e3f5eb387362	2025-10-23	Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	CVS Pharmacy, Inc	b57fc6c2-fbfc-24c3-e053-2995a90a3389	2025-10-16	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Amerisource Bergen	503f62e7-8ec8-4409-9697-4efef4ff7b15	2025-10-08	Warnings	Exact identifier application number: M009
Meclizine HCL 25 mg	MECLIZINE HCL	Proficient Rx LP	d08fa6f5-4293-4468-814e-7dccbd281209	2025-10-01	Warnings	Exact identifier application number: M009

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
JB937PER5C	DIMENHYDRINATE	523-87-5	DIMENHYDRINATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198603	dimenhyDRINATE 50 MG Oral Tablet	PSN	c25a7f2b-0f01-4ec0-8849-f08c23608d1d	16
198603	dimenhydrinate 50 MG Oral Tablet	SCD	c25a7f2b-0f01-4ec0-8849-f08c23608d1d	16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49035-981-12	49035098112	100 TABLET in 1 BOTTLE, PLASTIC (49035-981-12)	100 tablet	1992-12-01	0000-00-00	No	No	Current