UP AND UP CHILDRENS ALLERGY

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: UP AND UP CHILDRENS ALLERGY
Generic name: LORATADINE
Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
SPL set ID: a9f6ae02-cf29-4111-99e7-7e6b1ecb88f0
SPL ID: 36a8b979-6403-4545-82e0-d3bccdd2654e
Version: 2
Effective date: 2024-07-31
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:25:27

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	075728	derived:openfda.application_number
application number		ANDA075728	openfda.application_number
brand name		UP AND UP CHILDRENS ALLERGY	openfda.brand_name
generic name		LORATADINE	openfda.generic_name
manufacturer name		Target Corporation	openfda.manufacturer_name
ndc	package	82442-207-26	openfda.package_ndc
ndc	product	82442-207	openfda.product_ndc
ndc11	package	82442020726	derived:openfda.package_ndc
rxcui		692783	openfda.rxcui
spl id		36a8b979-6403-4545-82e0-d3bccdd2654e	id
spl set id		a9f6ae02-cf29-4111-99e7-7e6b1ecb88f0	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.