All Day Allergy Relief
- Product NDC
- 63868-107
- 11-digit product format
- 638680107
- Labeler code
- 63868
- Product ID
- 63868-107_de19d595-cba1-427e-8aa3-6455c00191f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- NDA022429
- Marketing category
- NDA
- Marketing start
- 2013-03-03
- Marketing end
- 2020-12-31
- 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