🇺🇸
United States · US · US:11673-612_244b9b86-cddc-46fb-8f03-312a3fed96d1
up and up allergy relief
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc1111673612031 BOTTLE in 1 CARTON (11673-612-03) / 70 TABLET in 1 BOTTLE
- ndc1111673612651 BOTTLE in 1 CARTON (11673-612-65) / 30 TABLET in 1 BOTTLE
- ndc111167361278100 TABLET in 1 BOTTLE (11673-612-78)
- ndc1111673612821 BOTTLE in 1 CARTON (11673-612-82) / 200 TABLET in 1 BOTTLE
- ndc1111673612871 BOTTLE in 1 CARTON (11673-612-87) / 300 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A076301
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": {
"51c0a953-93cb-4d0a-b51c-02d9482d1746": {
"match": "brand_token",
"title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
"spl_version": "12",
"published_date": "2026-05-13"
}
},
"productid": "11673-612_244b9b86-cddc-46fb-8f03-312a3fed96d1",
"productndc": "11673-612",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "076301",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Jun 25, 2004"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "up and up allergy relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA076301",
"marketing_category": "ANDA",
"nonproprietary_name": "Loratadine",
"start_marketing_date": "20120326",
"active_numerator_strength": "10"
}Related drugs
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