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United States · US · US:42507-458_a9ba17ab-f223-4850-a8c4-96ae247ed081
All Day Allergy
Orange BookUNIISPLATC R06AE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHyVee Inc
CountryUS (United States)
ATC codeR06AE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc1142507458391 BOTTLE in 1 CARTON (42507-458-39) / 30 TABLET, FILM COATED in 1 BOTTLE (42507-458-30)
- ndc1142507458721 BOTTLE in 1 CARTON (42507-458-72) / 60 TABLET, FILM COATED in 1 BOTTLE (42507-458-60)
- ndc1142507458751 BOTTLE in 1 CARTON (42507-458-75) / 90 TABLET, FILM COATED in 1 BOTTLE (42507-458-90)
- ndc1142507458871 BOTTLE in 1 CARTON (42507-458-87) / 300 TABLET, FILM COATED in 1 BOTTLE (42507-458-00)
- ndc1142507458951 BOTTLE in 1 CARTON (42507-458-95) / 45 TABLET, FILM COATED in 1 BOTTLE (42507-458-45)
Annotations
UNII (FDA Substance ID)
64O047KTOA
CETIRIZINE HYDROCHLORIDE
RxCUI 203150
Orange Book
A078336
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "64O047KTOA",
"rxcui": "203150",
"inchikey": "PGLIUCLTXOYQMV-UHFFFAOYSA-N",
"display_name": "CETIRIZINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"8889af37-8345-4358-994d-7d8b847f4874": {
"match": "brand_token",
"title": "ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [HYVEE INC]",
"spl_version": "6",
"published_date": "2026-05-13"
}
},
"productid": "42507-458_a9ba17ab-f223-4850-a8c4-96ae247ed081",
"productndc": "42507-458",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "078336",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "5MG",
"product_no": "001",
"approval_date": "Dec 27, 2007"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "002",
"approval_date": "Dec 27, 2007"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "5MG",
"product_no": "003",
"approval_date": "Dec 27, 2007"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "004",
"approval_date": "Dec 27, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CETIRIZINE HYDROCHLORIDE",
"proprietary_name": "All Day Allergy",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078336",
"marketing_category": "ANDA",
"nonproprietary_name": "Cetirizine Hydrochloride",
"start_marketing_date": "19970828",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code R06AE.
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