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: Meijer, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: deecbf76-be1d-4b27-85c6-17cfb7e7d1a1
SPL ID: dfa09879-a814-421c-8ea8-09193bc1c09d
Version: 4
Effective date: 2024-07-25
Source export date: 2026-10-30
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:31:47

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		allergy relief	openfda.brand_name
generic name		FEXOFENADINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Meijer, Inc.	openfda.manufacturer_name
ndc	package	79481-0847-4	openfda.package_ndc
ndc	package	79481-0847-3	openfda.package_ndc
ndc	package	79481-0847-1	openfda.package_ndc
ndc	package	79481-0847-2	openfda.package_ndc
ndc	package	79481-0847-0	openfda.package_ndc
ndc	product	79481-0847	openfda.product_ndc
ndc11	package	79481084702	derived:openfda.package_ndc
ndc11	package	79481084701	derived:openfda.package_ndc
ndc11	package	79481084704	derived:openfda.package_ndc
ndc11	package	79481084700	derived:openfda.package_ndc
ndc11	package	79481084703	derived:openfda.package_ndc
rxcui		997420	openfda.rxcui
spl id		dfa09879-a814-421c-8ea8-09193bc1c09d	id
spl set id		deecbf76-be1d-4b27-85c6-17cfb7e7d1a1	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.