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United States · US · US:41250-506_c0c28d44-6450-45e5-b8e2-2ce0de892365
Allergy Relief
Orange BookUNIISPLATC R06AX26
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMEIJER, INC.
CountryUS (United States)
ATC codeR06AX26
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11412505061515 BLISTER PACK in 1 CARTON (41250-506-15) / 1 TABLET, COATED in 1 BLISTER PACK
- ndc1141250506301 BOTTLE, PLASTIC in 1 CARTON (41250-506-30) / 30 TABLET, COATED in 1 BOTTLE, PLASTIC
- ndc1141250506451 BOTTLE, PLASTIC in 1 CARTON (41250-506-45) / 45 TABLET, COATED in 1 BOTTLE, PLASTIC
- ndc1141250506901 BOTTLE, PLASTIC in 1 CARTON (41250-506-90) / 90 TABLET, COATED in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
2S068B75ZU
FEXOFENADINE HYDROCHLORIDE
RxCUI 236474
Orange Book
A204507
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2S068B75ZU",
"rxcui": "236474",
"inchikey": "RRJFVPUCXDGFJB-UHFFFAOYSA-N",
"display_name": "FEXOFENADINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"934c7b91-3cba-47f0-8efa-77216f3f15c4": {
"match": "brand_token",
"title": "ALLERGY RELIEF CHILDRENS (DIPHENHYDRAMINE HCL) TABLET, CHEWABLE [AMERISOURCE BERGEN]",
"spl_version": "14",
"published_date": "2026-06-01"
}
},
"productid": "41250-506_c0c28d44-6450-45e5-b8e2-2ce0de892365",
"productndc": "41250-506",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "204507",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "60MG",
"product_no": "002",
"approval_date": "Sep 16, 2015"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "180MG",
"product_no": "003",
"approval_date": "Sep 16, 2015"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "60MG",
"product_no": "004",
"approval_date": "Sep 16, 2015"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "180MG",
"product_no": "005",
"approval_date": "Sep 16, 2015"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "FEXOFENADINE HYDROCHLORIDE",
"proprietary_name": "Allergy Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA204507",
"marketing_category": "ANDA",
"nonproprietary_name": "Fexofenadine HCl",
"start_marketing_date": "20180331",
"active_numerator_strength": "180"
}Related drugs
Other records sharing ATC code R06AX26.
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