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: LORATADINE
Manufacturer: Allegiant Health
Product type: HUMAN OTC DRUG
SPL set ID: f0db3a13-43e6-4243-9a3a-7808ddd005e1
SPL ID: 1307fce8-d753-4df5-90f0-a902befdfe35
Version: 10
Effective date: 2020-06-16
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:45

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 2 · 47 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	210722	derived:openfda.application_number
application applno	ANDA	211718	derived:openfda.application_number
application number		ANDA211718	openfda.application_number
application number		ANDA210722	openfda.application_number
brand name		Loratadine 10mg	openfda.brand_name
brand name		Allergy Relief	openfda.brand_name
generic name		LORATADINE	openfda.generic_name
generic name		LORATADINE 10MG	openfda.generic_name
manufacturer name		Allegiant Health	openfda.manufacturer_name
ndc	package	69168-414-99	openfda.package_ndc
ndc	package	69168-475-05	openfda.package_ndc
ndc	package	69168-475-17	openfda.package_ndc
ndc	package	69168-475-99	openfda.package_ndc
ndc	package	69168-475-60	openfda.package_ndc
ndc	package	69168-414-03	openfda.package_ndc
ndc	package	69168-414-09	openfda.package_ndc
ndc	package	69168-414-02	openfda.package_ndc
ndc	package	69168-414-60	openfda.package_ndc
ndc	package	69168-414-30	openfda.package_ndc
ndc	package	69168-475-30	openfda.package_ndc
ndc	package	69168-475-08	openfda.package_ndc
ndc	package	69168-475-02	openfda.package_ndc
ndc	package	69168-414-08	openfda.package_ndc
ndc	package	69168-414-17	openfda.package_ndc
ndc	package	69168-475-09	openfda.package_ndc
ndc	product	69168-414	openfda.product_ndc
ndc	product	69168-475	openfda.product_ndc
ndc11	package	69168041402	derived:openfda.package_ndc
ndc11	package	69168041430	derived:openfda.package_ndc
ndc11	package	69168047517	derived:openfda.package_ndc
ndc11	package	69168047599	derived:openfda.package_ndc
ndc11	package	69168047530	derived:openfda.package_ndc
ndc11	package	69168047505	derived:openfda.package_ndc
ndc11	package	69168047509	derived:openfda.package_ndc
ndc11	package	69168047502	derived:openfda.package_ndc
ndc11	package	69168041403	derived:openfda.package_ndc
ndc11	package	69168041417	derived:openfda.package_ndc
ndc11	package	69168047508	derived:openfda.package_ndc
ndc11	package	69168041408	derived:openfda.package_ndc
ndc11	package	69168047560	derived:openfda.package_ndc

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 liver or kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed. Taking more than directed may cause drowsiness. Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. Pregnancy/Breastfeeding ask a health professional before use. Keep out of reach of children In case of accidental overdose, contact a doctor or Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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