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United States · US · US:55910-985_31de3e6f-53da-4472-be5f-e512e7879420
All Day Allergy Relief
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDolgencorp, Inc. (DOLLAR GENERAL & REXALL)
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1155910985301 BOTTLE, PLASTIC in 1 BOX (55910-985-30) / 30 TABLET in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A075209
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7AJO3BO7QN",
"rxcui": "28889",
"inchikey": "JCCNYMKQOSZNPW-UHFFFAOYSA-N",
"display_name": "LORATADINE",
"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": "55910-985_31de3e6f-53da-4472-be5f-e512e7879420",
"productndc": "55910-985",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "075209",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Jan 21, 2003"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "All Day Allergy Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075209",
"marketing_category": "ANDA",
"nonproprietary_name": "Loratadine",
"start_marketing_date": "20231001",
"active_numerator_strength": "10"
}Related drugs
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