All Day Allergy

Product NDC
30142-211
11-digit product format
301420211
Labeler code
30142
Product ID
30142-211_9c833d2f-06f0-4f62-9d4d-04df28329dae
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine HCl
Dosage form
CAPSULE
Route
ORAL
Labeler
The Kroger Co.
Application
NDA022429
Marketing category
NDA
Marketing start
2013-12-30
Marketing end
2025-02-28
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
30142-211-25301420211251 BOTTLE, PLASTIC in 1 PACKAGE (30142-211-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC2013-12-300000-00-00NoNoCurrent
30142-211-40301420211401 BOTTLE, PLASTIC in 1 PACKAGE (30142-211-40) > 40 CAPSULE in 1 BOTTLE, PLASTIC2013-12-300000-00-00NoNoCurrent
30142-211-50301420211501 BOTTLE, PLASTIC in 1 PACKAGE (30142-211-50) > 50 CAPSULE in 1 BOTTLE, PLASTIC2013-12-300000-00-00NoNoCurrent