equate 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: equate loratadine
Generic name: LORATADINE
Manufacturer: WALMART INC.
Product type: HUMAN OTC DRUG
SPL set ID: 882dc99b-22d2-4f3e-8613-9ac8d9c5d910
SPL ID: ad482ac7-e600-455e-a6f4-44696f7a1784
Version: 2
Effective date: 2025-10-14
Source export date: 2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:26:29

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	076011	derived:openfda.application_number
application number		ANDA076011	openfda.application_number
brand name		equate loratadine	openfda.brand_name
generic name		LORATADINE	openfda.generic_name
manufacturer name		WALMART INC.	openfda.manufacturer_name
ndc	package	79903-381-10	openfda.package_ndc
ndc	product	79903-381	openfda.product_ndc
ndc11	package	79903038110	derived:openfda.package_ndc
rxcui		311373	openfda.rxcui
spl id		ad482ac7-e600-455e-a6f4-44696f7a1784	id
spl set id		882dc99b-22d2-4f3e-8613-9ac8d9c5d910	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.