Non-Drowsy Allergy Relief, 24-7 Life

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: Non-Drowsy Allergy Relief, 24-7 Life
Generic name: LORATADINE TABLET
Manufacturer: Lil' Drug Store Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 031ecc85-8324-4505-e063-6294a90a580b
SPL ID: 15c13bca-4dc5-07ec-e063-6394a90a5c5f
Version: 2
Effective date: 2024-04-10
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:17:52

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	210722	derived:openfda.application_number
application number		ANDA210722	openfda.application_number
brand name		Non-Drowsy Allergy Relief, 24-7 Life	openfda.brand_name
generic name		LORATADINE TABLET	openfda.generic_name
manufacturer name		Lil' Drug Store Products, Inc.	openfda.manufacturer_name
ndc	package	66715-6551-5	openfda.package_ndc
ndc	package	66715-6551-3	openfda.package_ndc
ndc	product	66715-6551	openfda.product_ndc
ndc11	package	66715655105	derived:openfda.package_ndc
ndc11	package	66715655103	derived:openfda.package_ndc
rxcui		311372	openfda.rxcui
spl id		15c13bca-4dc5-07ec-e063-6394a90a5c5f	id
spl set id		031ecc85-8324-4505-e063-6294a90a580b	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 Warnings Do not use 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 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 When using this product do not take more than directed. Taking more than directed may cause drowsiness. Stop use and ask a doctor if Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children 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.