Meclizine Hydrochloride

Product NDC: 68071-2574
11-digit product format: 680712574
Labeler code: 68071
Product ID: 68071-2574_49617f72-cc26-7c0d-e063-6294a90ac558
Type: HUMAN OTC DRUG
Nonproprietary name: Meclizine Hydrochloride
Dosage form: TABLET, CHEWABLE
Route: ORAL
Labeler: NuCare Pharmaceuticals,Inc.
Application: M009
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-10-30
Substance: MECLIZINE HYDROCHLORIDE
Active strength: 25 mg/1
Pharmacologic classes: Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 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	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	68071-2574-2	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	68071-2574-3	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	68071-2574-6	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	68071-2574-2	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	68071-2574-3	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	68071-2574-6	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	68071-2574-2	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	68071-2574-3	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	68071-2574-6	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	68071-2574-2	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	68071-2574-3	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	68071-2574-6	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	68071-2574-2	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	68071-2574-3	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	68071-2574-6	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	68071-2574-2	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	68071-2574-3	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	68071-2574-6	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	68071-2574-2	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	68071-2574-6	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	68071-2574-3	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	68071-2574-2	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	68071-2574-6	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	68071-2574-3	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	68071-2574-2	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	68071-2574-6	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	68071-2574-3	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Meclizine Hydrochloride
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MECLIZINE HYDROCHLORIDE	25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
HDP7W44CIO	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
995632	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
d0d8b376-8fe9-8776-e053-2a95a90ae651	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ac6963c4-31c6-325f-ee58-83a0a06597ad	Product name	5	20221206

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
68071-2574-2	2026-01-27	5172C- Rubgy
68071-2574-3	2026-01-27	5172C- Rubgy
68071-2574-6	2026-01-27	5172C- Rubgy
68071-2574-2	2025-01-30	5172C- Rubgy
68071-2574-3	2025-01-30	5172C- Rubgy
68071-2574-6	2025-01-30	5172C- Rubgy
68071-2574-2	2023-04-26	5172C- Rubgy
68071-2574-3	2023-04-26	5172C- Rubgy
68071-2574-6	2023-04-26	5172C- Rubgy
68071-2574-2	2023-01-30	5172C- Rubgy
68071-2574-3	2023-01-30	5172C- Rubgy
68071-2574-6	2023-01-30	5172C- Rubgy

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68071-2574-2	Meclizine Hydrochloride	20 in 1 BOTTLE	TABLET, CHEWABLE	20	6
68071-2574-3	Meclizine Hydrochloride	30 in 1 BOTTLE	TABLET, CHEWABLE	30	6
68071-2574-6	Meclizine Hydrochloride	60 in 1 BOTTLE	TABLET, CHEWABLE	60	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68071-2574	MECLIZINE HYDROCHLORIDE TABLET, CHEWABLE [NUCARE PHARMACEUTICALS,INC.]	5	Current NDC, Legacy NDC, 3 package rows	20230920_d0d8b376-8fe9-8776-e053-2a95a90ae651.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 4 of 6 · 107 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dramamine for Kids	DIMENHYDRINATE	Medtech Products Inc.	12bc3f17-ed62-4d0d-9b1e-3835579e711b	2025-09-10	Warnings	Exact identifier application number: M009
Medique Medi-Meclizine	MECLIZINE HCL	Unifirst First Aid Corporation	b3fec2df-c41d-0b56-e053-2995a90a35e8	2025-09-09	Warnings	Exact identifier application number: M009
Motion Sickness Relief	MECLIZINE HYDROCHLORIDE	TARGET CORPORATION	36ba2950-4a09-e5de-e063-6394a90a1771	2025-09-04	Warnings	Exact identifier application number: M009
MECLIZINE	MECLIZINE HCL 12.5 MG	Advanced Rx LLC	032a89f2-17e7-45d2-94a1-cc7a601ebdee	2025-09-01	Warnings	Exact identifier application number: M009
Dimenhydrinate	DIMENHYDRINATE	Major Pharmaceuticals	78d22836-a442-7c0c-e053-2991aa0a62f3	2025-08-13	Warnings	Exact identifier application number: M009
MQ Motion Patch	MOTION PATCH	Zhengzhou Miaoqi Medical Technology Co., Ltd.	3a70bc22-8e31-2d4c-e063-6394a90a3b24	2025-07-21	Warnings	Exact identifier application number: M009
Bangbrek Bee Venom Wart Corn Callus Remover	SALICYLIC ACID 17%	Brilliance Trade LLC	377946a0-0e8c-70f4-e063-6294a90a1d85	2025-06-20	Warnings	Exact identifier application number: M009
Dramamine for Kids	DIMENHYDRINATE	Medtech Products Inc.	48e2e9ef-4c88-42ef-b825-d1b007475275	2025-05-06	Warnings	Exact identifier application number: M009
BONINE MAX	MECLIZINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	7326a47e-284e-4b6f-8eb0-7933dc1e3f0d	2025-04-11	Warnings	Exact identifier application number: M009
Meclizine HCL 25 mg	MECLIZINE HCL	Bryant Ranch Prepack	d1c58a74-5455-4a07-bcb6-cc114032ed12	2025-03-31	Warnings	Exact identifier application number: M009
BONINE	MECLIZINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	ad3d66ca-a52c-43ba-b9e2-6269b8a413a9	2025-03-21	Warnings	Exact identifier application number: M009
BONINE	MECLIZINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	0b2ea6b8-b342-4940-8922-898758fbeb31	2025-03-21	Warnings	Exact identifier application number: M009
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Walgreen Company	ecf8d05e-0e77-f3e8-e053-2a95a90a6604	2025-03-11	Warnings	Exact identifier application number: M009
MECLIZINE	MECLIZINE HCL 25MG	PD-Rx Pharmaceuticals, Inc.	cf79ac74-017e-4fb4-85d3-4ea944080e89	2025-03-06	Warnings	Exact identifier application number: M009
HIONFURT Motion Sickness	MOTION SICKNESS NATURAL HERBAL PLANT	Puning Huiyu E-Commerce Co., Ltd.	2e2c9073-1dcf-a3e8-e063-6394a90a6ee3	2025-02-15	Warnings	Exact identifier application number: M009
HIONFURT Motion Sickness	MOTION SICKNESS NATURAL HERBAL PLANT LEMON	Puning Huiyu E-Commerce Co., Ltd.	2e2b3729-f8b0-605f-e063-6294a90a90c8	2025-02-15	Warnings	Exact identifier application number: M009
HIONFURT Motion Sickness	MOTION SICKNESS NATURAL HERBAL PLANT LAVENDER	Puning Huiyu E-Commerce Co., Ltd.	2e30b09d-838d-59fb-e063-6394a90aa984	2025-02-15	Warnings	Exact identifier application number: M009
HIONFURT Motion Sickness	MOTION SICKNESS PREVENT NAUSEA,DIZZINESS VOMITING	Puning Huiyu E-Commerce Co., Ltd.	2e31419e-3ccd-d7b5-e063-6394a90ac765	2025-02-15	Warnings	Exact identifier application number: M009
Dramamine for Kids	DIMENHYDRINATE	Medtech Products Inc.	3ccd6eb4-ba7e-4a6a-abb9-a6ef3196240c	2025-02-12	Warnings	Exact identifier application number: M009
Motion Sickness	MOTION SICKNESS NATURAL HERBAL PLANT	Puning Huiyu E-Commerce Co., Ltd.	2db09ade-c94b-5f5f-e063-6394a90af9dc	2025-02-09	Warnings	Exact identifier application number: M009

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
HDP7W44CIO	MECLIZINE HYDROCHLORIDE	31884-77-2	MECLIZINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
995632	meclizine HCl 25 MG Chewable Tablet	PSN	d0d8b376-8fe9-8776-e053-2a95a90ae651	6
995632	meclizine hydrochloride 25 MG Chewable Tablet	SCD	d0d8b376-8fe9-8776-e053-2a95a90ae651	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
68071-2574-2	68071257402	20 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-2)	2021-11-15	0000-00-00	No	No	Current
68071-2574-3	68071257403	30 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-3)	2021-11-15	0000-00-00	No	No	Current
68071-2574-6	68071257406	60 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-6)	2021-11-15	0000-00-00	No	No	Current