🇺🇸
United States · US · US:30142-723_84ae0ea9-82ae-4f98-a919-56c004444596
childrens allergy relief
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKroger Company
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1130142723001 BOTTLE in 1 CARTON (30142-723-00) / 118 mL in 1 BOTTLE
- ndc1130142723341 BOTTLE in 1 CARTON (30142-723-34) / 240 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A075728
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": {
"436c0126-4ff3-c082-e063-6294a90a3d72": {
"match": "brand_token",
"title": "CHILDRENS IBUPROFEN (IBUPROFEN) SUSPENSION [KESIN PHARMA CORPORATION]",
"spl_version": "2",
"published_date": "2026-06-01"
}
},
"productid": "30142-723_84ae0ea9-82ae-4f98-a919-56c004444596",
"productndc": "30142-723",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "075728",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "1MG/ML",
"product_no": "001",
"approval_date": "Aug 20, 2004"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "childrens allergy relief",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA075728",
"marketing_category": "ANDA",
"nonproprietary_name": "loratadine",
"start_marketing_date": "20200730",
"active_numerator_strength": "5"
}Related drugs
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