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: Publix Super Markets Inc
Product type: HUMAN OTC DRUG
SPL set ID: 76014f1e-fa48-4d64-9ce6-1eaebd0419fc
SPL ID: bdd76b8f-ab6c-477a-81d1-74256944dd62
Version: 2
Effective date: 2022-01-21
Source export date: 2026-11-06
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:05:27

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 · 16 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		Publix Super Markets Inc	openfda.manufacturer_name
ndc	package	56062-847-95	openfda.package_ndc
ndc	package	56062-847-22	openfda.package_ndc
ndc	package	56062-847-39	openfda.package_ndc
ndc	product	56062-847	openfda.product_ndc
ndc11	package	56062084722	derived:openfda.package_ndc
ndc11	package	56062084739	derived:openfda.package_ndc
ndc11	package	56062084795	derived:openfda.package_ndc
rxcui		997420	openfda.rxcui
spl id		bdd76b8f-ab6c-477a-81d1-74256944dd62	id
spl set id		76014f1e-fa48-4d64-9ce6-1eaebd0419fc	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.