Dramamine for Kids

Product NDC: 63029-904
Requested package NDC: 63029-904-01
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 · 20 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	`9bebd1f3094a…`	`5416666fcb17…`

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 1 of 6 · 116 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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
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
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
Motion Sickness	DIMENHYDRINATE	Geiss, Destin & Dunn Inc.	fdb683c5-ff7f-4b93-9892-670cf1f29f2a	2026-06-15	Warnings	Exact identifier application number: M009
Dimenhydrinate	DIMENHYDRINATE	CVS Pharmacy, Inc.	6dfc5cb4-af0c-56c9-e053-2a91aa0a5d56	2026-06-12	Warnings	Exact identifier application number: M009
Driminate	DIMENHYDRINATE	Major Pharmaceuticals	d2967f78-41ee-4c30-8b47-0757df9f3d91	2026-06-10	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Amerisource Bergen	c4077301-db6c-473d-beb3-232d7134a13a	2026-06-03	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Walgreen Company	761b7f9d-eaa1-47f0-89d9-c2da0e364a8b	2026-05-18	Warnings	Exact identifier application number: M009
Motion Sickness	MECLIZINE HCL	Strategic Sourcing Services LLC	550b803c-a038-455c-908a-a6244c0952ba	2026-05-12	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE	Valu Merchandisers Company	56c26102-8d39-458e-b076-3fe67456a4c0	2026-04-16	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	DOLGENCORP, LLC	1616c540-dcd9-46f1-823f-27b67ef488d2	2026-04-16	Warnings	Exact identifier application number: M009
Motion Sickness	DIMENHYDRINATE	Strategic Sourcing Services LLC	be8f91d4-6e4f-4d47-93e9-7fb91160b7df	2026-04-02	Warnings	Exact identifier application number: M009
Meclizine HCL 12.5 mg	MECLIZINE HCL 12.5 MG	Proficient Rx LP	3ffa63f2-ea06-4be0-9f59-162c2a9604fc	2026-04-01	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HCL	Meijer Distribution Inc	1ac451c4-2467-46d6-bc0d-f6368699d168	2026-03-23	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