CareOne Allergy Relief 24 Hour

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: CareOne Allergy Relief 24 Hour
Generic name: LORATADINE
Manufacturer: American Sales Company
Product type: HUMAN OTC DRUG
SPL set ID: bbd5424f-fa5b-4955-8542-7011b19400ea
SPL ID: 0a1c2126-c09e-4f8c-9aad-6e1aaf8bb4e7
Version: 13
Effective date: 2026-07-01
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:25

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 · 32 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		CareOne Allergy Relief 24 Hour	openfda.brand_name
generic name		LORATADINE	openfda.generic_name
manufacturer name		American Sales Company	openfda.manufacturer_name
ndc	package	41520-612-46	openfda.package_ndc
ndc	package	41520-612-03	openfda.package_ndc
ndc	package	41520-612-65	openfda.package_ndc
ndc	package	41520-612-82	openfda.package_ndc
ndc	package	41520-612-95	openfda.package_ndc
ndc	package	41520-612-72	openfda.package_ndc
ndc	package	41520-612-60	openfda.package_ndc
ndc	package	41520-612-76	openfda.package_ndc
ndc	package	41520-612-75	openfda.package_ndc
ndc	package	41520-612-78	openfda.package_ndc
ndc	package	41520-612-58	openfda.package_ndc
ndc	product	41520-612	openfda.product_ndc
ndc11	package	41520061272	derived:openfda.package_ndc
ndc11	package	41520061260	derived:openfda.package_ndc
ndc11	package	41520061246	derived:openfda.package_ndc
ndc11	package	41520061203	derived:openfda.package_ndc
ndc11	package	41520061258	derived:openfda.package_ndc
ndc11	package	41520061276	derived:openfda.package_ndc
ndc11	package	41520061278	derived:openfda.package_ndc
ndc11	package	41520061275	derived:openfda.package_ndc
ndc11	package	41520061295	derived:openfda.package_ndc
ndc11	package	41520061282	derived:openfda.package_ndc
ndc11	package	41520061265	derived:openfda.package_ndc
rxcui		311372	openfda.rxcui
spl id		0a1c2126-c09e-4f8c-9aad-6e1aaf8bb4e7	id
spl set id		bbd5424f-fa5b-4955-8542-7011b19400ea	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.