Leader 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: Leader Allergy Relief
Generic name: LORATADINE
Manufacturer: Cardinal Health 110, LLC. dba Leader
Product type: HUMAN OTC DRUG
SPL set ID: 6f5134c6-ece6-4e35-a0c3-13e0dfa173fa
SPL ID: ef5ff212-8517-4598-9876-2ba32b9d360b
Version: 6
Effective date: 2025-04-01
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 06:04:42

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	076301	derived:openfda.application_number
application number		ANDA076301	openfda.application_number
brand name		Leader Allergy Relief	openfda.brand_name
generic name		LORATADINE	openfda.generic_name
manufacturer name		Cardinal Health 110, LLC. dba Leader	openfda.manufacturer_name
ndc	package	70000-0213-3	openfda.package_ndc
ndc	package	70000-0213-4	openfda.package_ndc
ndc	package	70000-0213-7	openfda.package_ndc
ndc	package	70000-0213-5	openfda.package_ndc
ndc	package	70000-0213-2	openfda.package_ndc
ndc	package	70000-0213-1	openfda.package_ndc
ndc	package	70000-0213-6	openfda.package_ndc
ndc	product	70000-0213	openfda.product_ndc
ndc11	package	70000021305	derived:openfda.package_ndc
ndc11	package	70000021302	derived:openfda.package_ndc
ndc11	package	70000021304	derived:openfda.package_ndc
ndc11	package	70000021303	derived:openfda.package_ndc
ndc11	package	70000021307	derived:openfda.package_ndc
ndc11	package	70000021301	derived:openfda.package_ndc
ndc11	package	70000021306	derived:openfda.package_ndc
rxcui		311372	openfda.rxcui
spl id		ef5ff212-8517-4598-9876-2ba32b9d360b	id
spl set id		6f5134c6-ece6-4e35-a0c3-13e0dfa173fa	set_id
unii		7AJO3BO7QN	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 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. 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.