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United States · US · US:70000-0362_e888ebac-b741-9f96-5cd8-edfbad1a721d
24HR Allergy Relief
Orange BookUNIISPLATC R06AE09
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLEADER/ Cardinal Health 110, Inc.
CountryUS (United States)
ATC codeR06AE09
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1170000036212 BLISTER PACK in 1 CARTON (70000-0362-1) / 5 TABLET, COATED in 1 BLISTER PACK
- ndc1170000036221 BOTTLE in 1 CARTON (70000-0362-2) / 35 TABLET, COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
SOD6A38AGA
LEVOCETIRIZINE DIHYDROCHLORIDE
RxCUI 402349
Orange Book
A210375
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SOD6A38AGA",
"rxcui": "402349",
"inchikey": "PGLIUCLTXOYQMV-GHVWMZMZSA-N",
"display_name": "LEVOCETIRIZINE DIHYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"8917abc8-d391-89d1-ef3b-19e1702bc83d": {
"match": "brand_token",
"title": "24HR ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE) TABLET [LEADER/ CARDINAL HEALTH 110, INC.]",
"spl_version": "6",
"published_date": "2026-03-30"
}
},
"productid": "70000-0362_e888ebac-b741-9f96-5cd8-edfbad1a721d",
"productndc": "70000-0362",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "210375",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "5MG",
"product_no": "001",
"approval_date": "Jan 19, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LEVOCETIRIZINE DIHYDROCHLORIDE",
"proprietary_name": "24HR Allergy Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210375",
"marketing_category": "ANDA",
"nonproprietary_name": "levocetirizine dihydrochloride",
"start_marketing_date": "20180312",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code R06AE09.
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