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United States · US · US:59726-741_66c83cae-4168-4f79-8ce5-6f7b54703a7a
All Day Allergy Relief
Orange BookUNIISPLATC R06AE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerP & L Development, LLC
CountryUS (United States)
ATC codeR06AE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1159726741121 BOTTLE, PLASTIC in 1 BOX (59726-741-12) / 12 CAPSULE in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
64O047KTOA
CETIRIZINE HYDROCHLORIDE
RxCUI 203150
Orange Book
A207235
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": "59726-741_66c83cae-4168-4f79-8ce5-6f7b54703a7a",
"productndc": "59726-741",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "207235",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Aug 12, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CETIRIZINE HYDROCHLORIDE",
"proprietary_name": "All Day Allergy Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA207235",
"marketing_category": "ANDA",
"nonproprietary_name": "Cetirizine HCl",
"start_marketing_date": "20210129",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code R06AE.
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