Dramamine for Kids

Product NDC: 63029-904
11-digit product format: 630290904
Labeler code: 63029
Product ID: 63029-904_5bdaae92-e9c3-401c-a31c-5d0218b0481f
Type: HUMAN OTC DRUG
Nonproprietary name: Dimenhydrinate
Dosage form: TABLET, CHEWABLE
Route: ORAL
Labeler: Medtech Products Inc.
Application: M009
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-02-15
Marketing end: 2028-05-01
Substance: DIMENHYDRINATE
Active strength: 25 mg/1
Pharmacologic classes: Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag: No
Current FDA listing: Yes

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 · 40 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
2025-08-27 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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`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	63029-904-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	63029-904-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	63029-904-01	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	63029-904-01	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	63029-904-01	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	63029-904-01	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	63029-904-01	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	63029-904-01	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	63029-904-01	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	63029-904-01	`9bebd1f3094a…`	`5416666fcb17…`

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: Dramamine for Kids

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DIMENHYDRINATE	25 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 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1245184	Internal RxNorm lookup
1245186	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
12bc3f17-ed62-4d0d-9b1e-3835579e711b	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
6084a4f4-5437-c9a5-caec-5361ee075a59	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508
90c5639a-61b0-88d6-ddcf-21888e94869a	Product name	1	20140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63029-904-01	2025-09-09	C162847	48780-1	9d75b9d0-3b32-f424-e053-dadaa90a57ce	Dramamine for Kids
63029-904-01	2020-01-31	C162847	48780-1	9d75b9d0-3b32-f424-e053-dadaa90a57ce	Dramamine for Kids

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63029-904-01	Dramamine for Kids	1 in 1 BLISTER PACK	TABLET, CHEWABLE	1		4
63029-904-01	Dramamine for Kids	8 in 1 CASE	TABLET, CHEWABLE	8		4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63029-904-01	EA - Each	63029-904	216a5c51-e4ee-4248-bf9f-63116c035968	1	2022-06-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIMENHYDRINATE	ACTIVE INGREDIENT	JB937PER5C	DRAMAMINE FOR KIDS (DIMENHYDRINATE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.]	3
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	DRAMAMINE FOR KIDS (DIMENHYDRINATE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.]	3
ASPARTAME	INACTIVE INGREDIENT	Z0H242BBR1	DRAMAMINE FOR KIDS (DIMENHYDRINATE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.]	3
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	DRAMAMINE FOR KIDS (DIMENHYDRINATE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	DRAMAMINE FOR KIDS (DIMENHYDRINATE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.]	3
SORBITOL	INACTIVE INGREDIENT	506T60A25R	DRAMAMINE FOR KIDS (DIMENHYDRINATE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63029-904	DRAMAMINE FOR KIDS (DIMENHYDRINATE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.]	3	Current NDC, Legacy NDC, 2 package rows	20121026_12bc3f17-ed62-4d0d-9b1e-3835579e711b.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
1245184	dimenhyDRINATE 25 MG Chewable Tablet	PSN	12bc3f17-ed62-4d0d-9b1e-3835579e711b	4
1245186	Dramamine 25 MG Chewable Tablet	PSN	12bc3f17-ed62-4d0d-9b1e-3835579e711b	4
1245186	dimenhydrinate 25 MG Chewable Tablet [Dramamine]	SBD	12bc3f17-ed62-4d0d-9b1e-3835579e711b	4
1245184	dimenhydrinate 25 MG Chewable Tablet	SCD	12bc3f17-ed62-4d0d-9b1e-3835579e711b	4
1245186	Dramamine 25 MG Chewable Tablet	SY	12bc3f17-ed62-4d0d-9b1e-3835579e711b	4
1245186	Dramamine for Kids 25 MG Chewable Tablet	SY	12bc3f17-ed62-4d0d-9b1e-3835579e711b	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63029-904-01	63029090401	1 CASE in 1 BLISTER PACK (63029-904-01) / 8 TABLET, CHEWABLE in 1 CASE	1 case	2012-02-15	2028-05-01	No	No	Historical