All Day Allergy Relief
- Product NDC
- 59726-041
- 11-digit product format
- 597260041
- Labeler code
- 59726
- Product ID
- 59726-041_a29feb09-6727-4001-a5d5-36a2d1e51725
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA207235
- Marketing category
- ANDA
- Marketing start
- 2018-01-31
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-041-10 | 59726004110 | 1 BOTTLE in 1 BOX (59726-041-10) > 10 CAPSULE in 1 BOTTLE | 1 bottle | 2018-01-31 | 0000-00-00 | No | No | Current |
| 59726-041-12 | 59726004112 | 1 BOTTLE in 1 BOX (59726-041-12) > 12 CAPSULE in 1 BOTTLE | 1 bottle | 2018-01-31 | 0000-00-00 | No | No | Current |
| 59726-041-25 | 59726004125 | 1 BOTTLE in 1 BOX (59726-041-25) > 25 CAPSULE in 1 BOTTLE | 1 bottle | 2018-01-31 | 0000-00-00 | No | No | Current |