Meclizine HCL 25 mg

Product NDC: 71205-606
11-digit product format: 712050606
Labeler code: 71205
Product ID: 71205-606_f7855d32-3393-4704-a412-b978bf4962cf
Type: HUMAN OTC DRUG
Nonproprietary name: Meclizine HCL
Dosage form: TABLET
Route: ORAL
Labeler: Proficient Rx LP
Application: M009
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-11-01
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

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 HCL 25 mg
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
d08fa6f5-4293-4468-814e-7dccbd281209	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71205-606-30	Meclizine HCL 25 mg	30 in 1 BOTTLE, PLASTIC	TABLET	30	4
71205-606-60	Meclizine HCL 25 mg	60 in 1 BOTTLE, PLASTIC	TABLET	60	4
71205-606-90	Meclizine HCL 25 mg	90 in 1 BOTTLE, PLASTIC	TABLET	90	4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71205-606-30	EA - Each	71205-606	89874bdc-fef7-4df4-8aa2-57fac60f86dc	1	2022-03-09

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71205-606	MECLIZINE HCL 25 MG (MECLIZINE HCL) TABLET [PROFICIENT RX LP]	3	Current NDC, Legacy NDC, 3 package rows	20240125_d08fa6f5-4293-4468-814e-7dccbd281209.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 ndc (product): 71205-606

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	d08fa6f5-4293-4468-814e-7dccbd281209	4
995632	meclizine hydrochloride 25 MG Chewable Tablet	SCD	d08fa6f5-4293-4468-814e-7dccbd281209	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71205-606-30	71205060630	30 TABLET in 1 BOTTLE, PLASTIC (71205-606-30)	30 tablet	2021-09-14	0000-00-00	No	No	Current
71205-606-60	71205060660	60 TABLET in 1 BOTTLE, PLASTIC (71205-606-60)	60 tablet	2021-09-14	0000-00-00	No	No	Current
71205-606-90	71205060690	90 TABLET in 1 BOTTLE, PLASTIC (71205-606-90)	90 tablet	2021-09-14	0000-00-00	No	No	Current