United States · FDA National Drug Code directory
All Day Allergy
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 42507-458_a9ba17ab-f223-4850-a8c4-96ae247ed081
- Product NDC
- 42507-458
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- HyVee Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19970828
- Source listing expiry
- 20271231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (42507-458-39) / 30 TABLET, FILM COATED in 1 BOTTLE (42507-458-30) · 42507-458-39
- 1 BOTTLE in 1 CARTON (42507-458-72) / 60 TABLET, FILM COATED in 1 BOTTLE (42507-458-60) · 42507-458-72
- 1 BOTTLE in 1 CARTON (42507-458-75) / 90 TABLET, FILM COATED in 1 BOTTLE (42507-458-90) · 42507-458-75
- 1 BOTTLE in 1 CARTON (42507-458-87) / 300 TABLET, FILM COATED in 1 BOTTLE (42507-458-00) · 42507-458-87
- 1 BOTTLE in 1 CARTON (42507-458-95) / 45 TABLET, FILM COATED in 1 BOTTLE (42507-458-45) · 42507-458-95
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →