good sense aller ease

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: good sense aller ease
Generic name: FEXOFENADINE HYDROCHLORIDE
Manufacturer: L. Perrigo Company
Product type: HUMAN OTC DRUG
SPL set ID: e533a008-b437-401e-ab50-bda31e6662d3
SPL ID: 5cd21fe5-5a25-4beb-a480-924996e65ee1
Version: 3
Effective date: 2025-10-09
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:45:08

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	212971	derived:openfda.application_number
application number		ANDA212971	openfda.application_number
brand name		good sense aller ease	openfda.brand_name
generic name		FEXOFENADINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		L. Perrigo Company	openfda.manufacturer_name
ndc	package	0113-0847-22	openfda.package_ndc
ndc	package	0113-0847-95	openfda.package_ndc
ndc	package	0113-0847-00	openfda.package_ndc
ndc	package	0113-0847-47	openfda.package_ndc
ndc	package	0113-0847-39	openfda.package_ndc
ndc	product	0113-0847	openfda.product_ndc
ndc11	package	00113084739	derived:openfda.package_ndc
ndc11	package	00113084700	derived:openfda.package_ndc
ndc11	package	00113084747	derived:openfda.package_ndc
ndc11	package	00113084795	derived:openfda.package_ndc
ndc11	package	00113084722	derived:openfda.package_ndc
rxcui		997420	openfda.rxcui
spl id		5cd21fe5-5a25-4beb-a480-924996e65ee1	id
spl set id		e533a008-b437-401e-ab50-bda31e6662d3	set_id
unii		2S068B75ZU	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 Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have kidney disease. Your doctor should determine if you need a different dose. When using this product • do not take more than directed • do not take at the same time as aluminum or magnesium antacids • do not take with fruit juices (see Directions) Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. 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 (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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