LORATADINE

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: LORATADINE
Generic name: LORATADINE
Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
SPL set ID: 0599cc64-419d-452f-ac50-ac0311006729
SPL ID: 4716c66e-ed8d-11bd-e063-6294a90a685c
Version: 3
Effective date: 2025-12-29
Source export date: 2026-11-06
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/5781d2d281f00c57d2634422e88d204f4ab5cf8444979f7006f538b3a4f26d3b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:32:55

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	206214	derived:openfda.application_number
application number		ANDA206214	openfda.application_number
brand name		LORATADINE	openfda.brand_name
generic name		LORATADINE	openfda.generic_name
manufacturer name		KROGER COMPANY	openfda.manufacturer_name
ndc	package	41226-686-30	openfda.package_ndc
ndc	product	41226-686	openfda.product_ndc
ndc11	package	41226068630	derived:openfda.package_ndc
rxcui		828269	openfda.rxcui
spl id		4716c66e-ed8d-11bd-e063-6294a90a685c	id
spl set id		0599cc64-419d-452f-ac50-ac0311006729	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

DO NOT USE IF YOU HAVE EVER HAD AN ALLERGIC REACTION TO THIS PRODUCT OR ANY OF ITS INGREDIENTS. 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.

Reported adverse events (FAERS/openFDA)#

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