Motion Sickness

Product NDC: 59779-198
11-digit product format: 597790198
Labeler code: 59779
Product ID: 59779-198_65260d76-468e-48bd-995b-17da38f17c99
Type: HUMAN OTC DRUG
Nonproprietary name: Dimenhydrinate
Dosage form: TABLET
Route: ORAL
Labeler: CVS Pharmacy
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	59779-198	59779-198-21	D	Discontinued by firm		2026-08-17

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 36 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59779-198-21	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59779-198-07	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59779-198-21	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59779-198-07	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	59779-198-21	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	59779-198-07	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	59779-198-21	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	59779-198-07	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	59779-198-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	59779-198-07	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	59779-198-21	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	59779-198-07	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	59779-198-21	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	59779-198-07	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	59779-198-21	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	59779-198-07	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59779-198-21	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59779-198-07	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59779-198-21	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59779-198-07	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	59779-198-21	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	59779-198-07	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	59779-198-21	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	59779-198-07	`557ba5c1ecfa…`	`9c80585c8c6e…`

Additional Listing Data#

Finished product: Yes
Brand name base: Motion Sickness
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
0998947c-cfba-497e-bf7a-9c7f8fff1764	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	SPL version
59779-198-02	Motion Sickness	2 in 1 CARTON	TABLET	2	16
59779-198-02	Motion Sickness	6 in 1 BLISTER PACK	TABLET	6	16
59779-198-07	Motion Sickness	6 in 1 BLISTER PACK	TABLET	6	16
59779-198-07	Motion Sickness	6 in 1 CARTON	TABLET	6	16
59779-198-21	Motion Sickness	1 in 1 CARTON	TABLET	1	16
59779-198-21	Motion Sickness	16 in 1 VIAL	TABLET	16	16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIMENHYDRINATE	ACTIVE INGREDIENT	JB937PER5C	MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	L11K75P92J	MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MOTION SICKNESS (DIMENHYDRINATE) TABLET [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7

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 · 117 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nausea Relief	MECLIZINE HCL	WALMART INC.	8010741e-61b2-4c1f-9f0e-21612878fa0e	2026-08-25	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
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 ndc (product): 59779-198
Motion Sickness Relief	MECLIZINE HCL	Topco Associates, LLC	307e3144-3b01-4bd0-9155-6b58fc4cab92	2026-07-09	Warnings	Exact identifier application number: M009
Less Drowsy Motion Sickness Relief	MECLIZINE HCL	Wal-Mart Stores Inc	277a6266-e641-4621-bbb9-64195d51b66a	2026-07-01	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
DRAMAMINE CHEWABLE ORANGE	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	30387e63-278d-412a-bcad-7965c7c0aea7	2026-06-23	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Wal-Mart Stores Inc	c25a7f2b-0f01-4ec0-8849-f08c23608d1d	2026-06-22	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Cardinal Health 110, LLC. DBA Leader	69099658-a584-49a9-8a95-de258a697c4f	2026-06-16	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Topco Associates, LLC	503a70db-d564-4ea0-851e-8ff617e70728	2026-06-16	Warnings	Exact identifier application number: M009
Motion Sickness	MECLIZINE HCL	ARMY AND AIR FORCE EXCHANGE SERVICE	20229ad5-cb28-4667-ab70-97a1102873a2	2026-06-16	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	0998947c-cfba-497e-bf7a-9c7f8fff1764	16
198603	dimenhydrinate 50 MG Oral Tablet	SCD	0998947c-cfba-497e-bf7a-9c7f8fff1764	16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59779-198-02	59779019802	2 BLISTER PACK in 1 CARTON (59779-198-02) / 6 TABLET in 1 BLISTER PACK	2 blister pack	1992-12-01		No	No	Current
59779-198-07	59779019807	6 BLISTER PACK in 1 CARTON (59779-198-07) / 6 TABLET in 1 BLISTER PACK	6 blister pack	1992-12-01	0000-00-00	No	No	Current
59779-198-21	59779019821	1 in 1 CARTON						Historical