Allergy Relief

Product NDC
68210-4169
11-digit product format
682104169
Labeler code
68210
Product ID
68210-4169_eecb8bbf-5943-4814-e053-2a95a90a88ce
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydraime HCl
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Spirit Pharmaceuticals LLC
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-11-16
Marketing end
0000-00-00
Substance
DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68210-4169-3Allergy Relief30 in 1 POUCHTABLET, FILM COATED306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68210-4169ALLERGY RELIEF (DIPHENHYDRAIME HCL) TABLET, FILM COATED [SPIRIT PHARMACEUTICALS LLC]6Legacy NDC, 1 package rows20241211_61c340e5-ace6-4ec1-9d3e-e965fca1263a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049630diphenhydrAMINE HCl 25 MG Oral TabletPSN61c340e5-ace6-4ec1-9d3e-e965fca1263a6
1049630diphenhydramine hydrochloride 25 MG Oral TabletSCD61c340e5-ace6-4ec1-9d3e-e965fca1263a6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68210-4169-36821041690330 TABLET, FILM COATED in 1 POUCH (68210-4169-3) 2021-11-160000-00-00NoNoCurrent