ALLERGY RELIEF

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: ALLERGY RELIEF
Generic name: FEXOFENADINE HYDROCHLORIDE
Manufacturer: YYBA CORP
Product type: HUMAN OTC DRUG
SPL set ID: a1e80757-346f-4d88-8da7-55583c3a902b
SPL ID: 4482573c-af39-436a-e063-6294a90ac4ea
Version: 8
Effective date: 2025-11-26
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:05:20

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	204507	derived:openfda.application_number
application number		ANDA204507	openfda.application_number
brand name		ALLERGY RELIEF	openfda.brand_name
generic name		FEXOFENADINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		YYBA CORP	openfda.manufacturer_name
ndc	package	73581-103-01	openfda.package_ndc
ndc	package	73581-103-20	openfda.package_ndc
ndc	package	73581-103-60	openfda.package_ndc
ndc	package	73581-103-10	openfda.package_ndc
ndc	product	73581-103	openfda.product_ndc
ndc11	package	73581010310	derived:openfda.package_ndc
ndc11	package	73581010360	derived:openfda.package_ndc
ndc11	package	73581010320	derived:openfda.package_ndc
ndc11	package	73581010301	derived:openfda.package_ndc
rxcui		997501	openfda.rxcui
spl id		4482573c-af39-436a-e063-6294a90ac4ea	id
spl set id		a1e80757-346f-4d88-8da7-55583c3a902b	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.

Reported adverse events (FAERS/openFDA)#

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