All Day Allergy
- Product NDC
- 37808-211
- 11-digit product format
- 378080211
- Labeler code
- 37808
- Product ID
- 37808-211_021ac2b4-0c97-41bf-bd32-ddc3b723e85d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- H E B
- Application
- NDA022429
- Marketing category
- NDA
- Marketing start
- 2013-10-09
- Marketing end
- 2024-01-05
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 37808-211-25 | 37808021125 | 1 BOTTLE in 1 BOX (37808-211-25) > 25 CAPSULE in 1 BOTTLE | 1 bottle | 2013-10-09 | 2024-01-05 | No | No | Current |