up and up allergy relief
- Product NDC
- 11673-690
- Requested package NDC
- 11673-690-78
- 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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-690 | UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [TARGET CORPORATION] | 9 | Legacy NDC | 20240719_0534134f-8baa-430c-bdd1-9b83cbc81703.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-690-78 | 11673069078 | 1 BOTTLE in 1 CARTON (11673-690-78) > 100 TABLET in 1 BOTTLE | 1 bottle | 2009-06-16 | 0000-00-00 | No | No | Current |