Meclizine HCL 25 mg

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Meclizine HCL 25 mg
Generic name: MECLIZINE HCL
Manufacturer: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
SPL set ID: d1c58a74-5455-4a07-bcb6-cc114032ed12
SPL ID: afe16058-294e-4e4f-9a1b-4af4e96eedea
Version: 5
Effective date: 2025-03-31
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:23

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M009	openfda.application_number
brand name		Meclizine HCL 25 mg	openfda.brand_name
generic name		MECLIZINE HCL	openfda.generic_name
manufacturer name		Bryant Ranch Prepack	openfda.manufacturer_name
ndc	package	71335-1607-8	openfda.package_ndc
ndc	package	71335-1607-3	openfda.package_ndc
ndc	package	71335-1607-7	openfda.package_ndc
ndc	package	71335-1607-2	openfda.package_ndc
ndc	package	71335-1607-4	openfda.package_ndc
ndc	package	71335-1607-1	openfda.package_ndc
ndc	package	71335-1607-5	openfda.package_ndc
ndc	package	71335-1607-0	openfda.package_ndc
ndc	package	71335-1607-9	openfda.package_ndc
ndc	package	71335-1607-6	openfda.package_ndc
ndc	product	71335-1607	openfda.product_ndc
ndc11	package	71335160703	derived:openfda.package_ndc
ndc11	package	71335160708	derived:openfda.package_ndc
ndc11	package	71335160700	derived:openfda.package_ndc
ndc11	package	71335160707	derived:openfda.package_ndc
ndc11	package	71335160701	derived:openfda.package_ndc
ndc11	package	71335160702	derived:openfda.package_ndc
ndc11	package	71335160709	derived:openfda.package_ndc
ndc11	package	71335160706	derived:openfda.package_ndc
ndc11	package	71335160705	derived:openfda.package_ndc
ndc11	package	71335160704	derived:openfda.package_ndc
rxcui		995632	openfda.rxcui
spl id		afe16058-294e-4e4f-9a1b-4af4e96eedea	id
spl set id		d1c58a74-5455-4a07-bcb6-cc114032ed12	set_id
unii		HDP7W44CIO	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers When using this prodcut you may get drowsy avoid alcoholic drinks alcohol, sedatives and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.