rexall sleep aid

Product NDC
55910-702
Requested package NDC
55910-702-78
11-digit product format
559100702
Labeler code
55910
Product ID
55910-702_af12b140-704c-45c4-800a-2aea2814faee
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydramine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Dolgencorp, LLC
Application
part338
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-09-29
Marketing end
0000-00-00
Substance
DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
25 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
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 packagepackage55910-70255910-702-78DDiscontinued by firm2026-10-12

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-702REXALL SLEEP AID (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [DOLGENCORP, LLC]4Legacy NDC20241009_90203b5d-cc75-4eee-913d-d6629199a015.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55910-702-78559100702781 BOTTLE in 1 CARTON (55910-702-78) > 100 TABLET in 1 BOTTLE1 bottle2010-09-290000-00-00NoNoCurrent