FDA.reportPublic FDA data

Allergy Relief

Product NDC
69842-174
Requested package NDC
69842-174-36
11-digit product format
698420174
Labeler code
69842
Product ID
69842-174_f5bb3121-f30f-45d9-a2b9-c4970137710e
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydramine HCl
Dosage form
SOLUTION
Route
ORAL
Labeler
CVS PHARMACY
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-01-26
Marketing end
0000-00-00
Substance
DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
50 mg/20mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage69842-17469842-174-36DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-174-36Allergy Relief1 in 1 CARTONSOLUTION18
69842-174-36Allergy Relief118 mL in 1 BOTTLE, PLASTICSOLUTION1188

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-174ALLERGY RELIEF (DIPHENHYDRAMINE HCL) SOLUTION [CVS PHARMACY]7Legacy NDC, 2 package rows20240918_3f05a2f5-b4e9-4f8c-8c3e-1338b4b741ae.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Allergy ReliefDIPHENHYDRAMINE HCLCVS PHARMACY3f05a2f5-b4e9-4f8c-8c3e-1338b4b741ae2025-09-23WarningsExact identifier
ndc (package): 69842-174-36
ndc (product): 69842-174
ndc11 (package): 69842017436

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049906diphenhydrAMINE HCl 12.5 MG in 5 mL Oral SolutionPSN3f05a2f5-b4e9-4f8c-8c3e-1338b4b741ae8
1049906diphenhydramine hydrochloride 2.5 MG/ML Oral SolutionSCD3f05a2f5-b4e9-4f8c-8c3e-1338b4b741ae8
1049906diphenhydramine HCl 12.5 MG per 5 ML Oral SolutionSY3f05a2f5-b4e9-4f8c-8c3e-1338b4b741ae8
1049906diphenhydramine hydrochloride 25 MG per 10 ML Oral SolutionSY3f05a2f5-b4e9-4f8c-8c3e-1338b4b741ae8
1049906diphenhydramine hydrochloride 50 MG per 20 ML Oral SolutionSY3f05a2f5-b4e9-4f8c-8c3e-1338b4b741ae8

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
69842-174-36698420174361 BOTTLE, PLASTIC in 1 CARTON (69842-174-36) > 118 mL in 1 BOTTLE, PLASTIC2021-01-260000-00-00NoNoCurrent