Up and Up Ultra Itchy Relief
- Product NDC
- 11673-672
- 11-digit product format
- 116730672
- Labeler code
- 11673
- Product ID
- 11673-672_97547147-f9d4-5afc-e053-2a95a90a8029
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tetrahydrozoline HCI and Zinc Sulfate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Target Corporation
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-09-20
- Marketing end
- 0000-00-00
- Substance
- TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE
- Active strength
- 1 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-672-05 | Up and Up Ultra Itchy Relief | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 2 |
| 11673-672-05 | Up and Up Ultra Itchy Relief | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-672 | UP AND UP ULTRA ITCHY RELIEF (TETRAHYDROZOLINE HCI AND ZINC SULFATE) SOLUTION/ DROPS [TARGET CORPORATION] | 2 | Legacy NDC, 2 package rows | 20191115_93010f79-e940-f064-e053-2a95a90a5c23.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-672-05 | 11673067205 | 1 BOTTLE, DROPPER in 1 CARTON (11673-672-05) > 15 mL in 1 BOTTLE, DROPPER | 2019-09-20 | 0000-00-00 | No | No | Current |