up and up
- Product NDC
- 11673-106
- 11-digit product format
- 116730106
- Labeler code
- 11673
- Product ID
- 11673-106_3d7eb25d-fe73-4084-b859-9e15cde547ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA201546
- Marketing category
- ANDA
- Marketing start
- 2011-05-20
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 11673-106-08 | up and up childrens all day allergy relief | 120 mL in 1 BOTTLE | SOLUTION | 120 | | 1 |
| 11673-106-08 | up and up childrens all day allergy relief | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-106 | UP AND UP CHILDRENS ALL DAY ALLERGY RELIEF (CETIRIZINE HYDROCHLORIDE) SOLUTION [TARGET CORPORATION] | 1 | Legacy NDC, 2 package rows | 20130618_89acf9af-d8e8-49ea-8e03-1bfb37089ca8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 11673-106-08 | 11673010608 | 120 mL in 1 BOTTLE | 120 ml | Historical |