FDA.reportPublic FDA data

up and up allergy relief

Product NDC
11673-690
Requested package NDC
11673-690-62
11-digit product format
116730690
Labeler code
11673
Product ID
11673-690_b316b001-b421-4364-aaf4-2cf525f3d055
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydramine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Target Corporation
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2009-06-12
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

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 packagepackage11673-69011673-690-62DDiscontinued by firm2026-10-20

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-690-622024-01-30C16284748780-11030e365-1f2e-111a-e063-dadaa90a10e2Target Corporation Allergy Relief Drug Facts
11673-690-782024-01-30C16284748780-11030e365-1f2e-111a-e063-dadaa90a10e2Target Corporation Allergy Relief Drug Facts
11673-690-872024-01-30C16284748780-11030e365-1f2e-111a-e063-dadaa90a10e2Target Corporation Allergy Relief Drug Facts

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
11673-690-78EA - Each11673-6909c43f0ac-02fe-4a32-840d-6ea31d1169e712016-05-16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DIPHENHYDRAMINE HYDROCHLORIDEACTIVE INGREDIENTTC2D6JAD40UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
DIPHENHYDRAMINEACTIVE MOIETY8GTS82S83MUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATEINACTIVE INGREDIENTO7TSZ97GEPUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
CROSPOVIDONEINACTIVE INGREDIENT68401960MKUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPUP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-690UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]9Legacy NDC20240719_0534134f-8baa-430c-bdd1-9b83cbc81703.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-690-621167306906224 BLISTER PACK in 1 CARTON (11673-690-62) > 1 TABLET in 1 BLISTER PACK24 blister pack2009-06-120000-00-00NoNoCurrent