NDC 11822-0475-01 - childrens allergy relief

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
11822-0475
Requested NDC
11822-0475-01
Package NDCs from labels
11822-0475-1, 11822-0475-0, 11822-0475-01
Manufacturer
Rite Aid Corporation
Effective date
2026-07-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
childrens allergy relief - Rite Aid CorporationRite Aid Corporation2026-07-24HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-0475-0childrens allergy relief1 in 1 CARTONSOLUTION15
11822-0475-0childrens allergy relief240 mL in 1 BOTTLESOLUTION2405
11822-0475-1childrens allergy relief1 in 1 CARTONSOLUTION15
11822-0475-1childrens allergy relief118 mL in 1 BOTTLESOLUTION1185

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0475CHILDRENS ALLERGY RELIEF (CETIRIZINE HCL) SOLUTION [RITE AID CORPORATION]5Current NDC, Legacy NDC, 4 package rows20250508_09474431-cf46-45da-8b20-9551ddea28a7.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 39 of 39 · 762 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cetirizine HydrochlorideCETIRIZINE HYDROCHLORIDESandoz Inc760dd0e4-280a-4d95-8938-cecaa7ec75f22013-06-03WarningsExact identifier
unii: 64O047KTOA
Cetirizine HydrochlorideCETIRIZINE HYDROCHLORIDEDr.Reddy's Laboratories Limitedde152651-bfcd-856a-8329-a2ac93a376bc2011-09-30WarningsExact identifier
unii: 64O047KTOA

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.