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 5 of 6 · 107 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Motion Sickness Relief	DIMENHYDRINATE 50 MG	TARGET CORPORATION	28586e9b-01e3-0b88-e063-6394a90af7e0	2025-01-29	Warnings	Exact identifier application number: M009
MECLIZINE	MECLIZINE HCL 12.5MG	Ulai Health LLC	d304e205-85fa-494a-9a68-ae6855b139b1	2025-01-20	Warnings	Exact identifier application number: M009
Meclizine HCL 12.5 mg	MECLIZINE HCL 12.5 MG	Reliable 1 Laboratories LLC	32832b0f-0b38-27ce-e054-00144ff8d46c	2025-01-15	Warnings	Exact identifier application number: M009
Meclizine HCL 25 mg	MECLIZINE HCL	Reliable 1 Laboratories LLC	32bdd802-16b0-184d-e054-00144ff88e88	2025-01-15	Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	APNAR PHARMA LP	e4d785a7-a688-3acb-e053-2a95a90a6d2e	2025-01-09	Boxed warning, Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	APNAR PHARMA LP	ed43bf21-f3da-245c-e053-2995a90a504c	2025-01-09	Boxed warning, Warnings	Exact identifier application number: M009
MECLIZINE	MECLIZINE HCL 12.5 MG	RUGBY LABORATORIES	8a234ce3-eb6b-49dd-9d78-7fc7bdd49d35	2024-12-20	Warnings	Exact identifier application number: M009
Meclizine	MECLIZINE HYDROCHLORIDE	Advanced Rx LLC	b0a2a1f7-354e-48bd-9e98-9207bf9f53fd	2024-11-27	Warnings	Exact identifier application number: M009
Dramamine, TRAVEL BASIX	DIMENHYDRINATE	Lil' Drug Store Products, Inc.	960a642b-ee7c-4e92-9b5f-930425682dac	2024-11-26	Warnings	Exact identifier application number: M009
Dramamine Less Drowsy, Lil Drug Store	MECLAZINE HYDROCHLORIDE TABLET	Lil' Drug Store Products, Inc.	275b3377-9280-c12c-e063-6294a90a5421	2024-11-20	Warnings	Exact identifier application number: M009
PhysiciansCare Motion Sickness	MECLIZINE HCL	Acme United Corporation	c4d3ea22-7c22-7311-e053-2a95a90a779c	2024-11-12	Warnings	Exact identifier application number: M009
DRAMAMINE - N	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	7fec7791-c242-4e43-8184-32820e657afb	2024-10-25	Warnings	Exact identifier application number: M009
DRAMAMINE	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	f8cf751a-9f19-4744-a350-cd22303435ee	2024-10-25	Warnings	Exact identifier application number: M009
Gravol	DIMENHYDRINATE	Church & Dwight Co., Inc.	d955f612-1265-f1be-e053-2995a90a5345	2024-07-18	Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	199ae195-4556-ee88-e063-6394a90a40d4	2024-06-10	Warnings	Exact identifier application number: M009
Gravol	DIMENHYDRINATE	Church & Dwight Co., Inc.	d941705f-12a1-4757-e053-2995a90ad3fa	2024-05-13	Warnings	Exact identifier application number: M009
Kids Gravol Chewables Motion Sickness Dimenhydrinate	DIMENHYDRINATE	Church & Dwight Co., Inc.	cf6de950-a157-4be2-a302-0dc19511d2f2	2024-03-01	Warnings	Exact identifier application number: M009
Gravol Chewables Motion Sickness Dimenhydrinate	DIMENHYDRINATE	Church & Dwight Co., Inc.	de5249f7-79fc-4f3c-965a-1e8ec978a0b7	2024-03-01	Warnings	Exact identifier application number: M009
Meclizine HCl	MECLIZINE HYDROCHLORIDE CHEWABLE	BluePoint Laboratories	d9cc2705-9dcc-0a73-e053-2995a90aafe6	2024-02-21	Warnings	Exact identifier application number: M009
Childrens Allergy	DIPHENHYDRAMINE HYDROCHLORIDE	DeMoulas Market Basket	fd04fb94-f581-4ca2-b7ac-20359093863e	2023-12-29	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