dg health 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: dg health allergy relief
Generic name: LORATADINE
Manufacturer: Dolgencorp Inc
Product type: HUMAN OTC DRUG
SPL set ID: dfc4b065-1980-48ec-9c3e-aaa4a42214d3
SPL ID: f7ea9f4d-11cc-4498-852b-3745cbb51b8b
Version: 11
Effective date: 2026-07-02
Source export date: 2026-11-06
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:03:15

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 · 20 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		dg health allergy relief	openfda.brand_name
generic name		LORATADINE	openfda.generic_name
manufacturer name		Dolgencorp Inc	openfda.manufacturer_name
ndc	package	55910-806-46	openfda.package_ndc
ndc	package	55910-806-49	openfda.package_ndc
ndc	package	55910-806-65	openfda.package_ndc
ndc	package	55910-806-72	openfda.package_ndc
ndc	package	55910-806-39	openfda.package_ndc
ndc	product	55910-806	openfda.product_ndc
ndc11	package	55910080665	derived:openfda.package_ndc
ndc11	package	55910080649	derived:openfda.package_ndc
ndc11	package	55910080646	derived:openfda.package_ndc
ndc11	package	55910080639	derived:openfda.package_ndc
ndc11	package	55910080672	derived:openfda.package_ndc
rxcui		311372	openfda.rxcui
spl id		f7ea9f4d-11cc-4498-852b-3745cbb51b8b	id
spl set id		dfc4b065-1980-48ec-9c3e-aaa4a42214d3	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.