up and up allergy relief
- Product NDC
- 11673-705
- 11-digit product format
- 116730705
- Labeler code
- 11673
- Product ID
- 11673-705_222512df-3f16-4cb5-ae1c-b554a7fc592e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA090254
- Marketing category
- ANDA
- Marketing start
- 2014-12-23
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-705 | UP AND UP ALLERGY RELIEF (CETIRIZINE HYDROCHLORIDE) SOLUTION [TARGET CORPORATION] | 3 | Legacy NDC | 20181217_15069389-9113-4ddd-92d0-fa6d667402cf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-705-26 | 11673070526 | 1 BOTTLE in 1 CARTON (11673-705-26) > 118 mL in 1 BOTTLE | 1 bottle | 2014-12-23 | 0000-00-00 | No | No | Current |