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United States · US · US:50090-4741_c01c6ad7-a304-4190-9d9e-cdef0dc8c6f5
CHILDRENS ALLERGY RELIEF
Orange BookUNIISPLATC R06AE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeR06AE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1150090474101 BOTTLE in 1 CARTON (50090-4741-0) / 118 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
64O047KTOA
CETIRIZINE HYDROCHLORIDE
RxCUI 203150
Orange Book
A210622
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "64O047KTOA",
"rxcui": "203150",
"inchikey": "PGLIUCLTXOYQMV-UHFFFAOYSA-N",
"display_name": "CETIRIZINE HYDROCHLORIDE",
"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": "50090-4741_c01c6ad7-a304-4190-9d9e-cdef0dc8c6f5",
"productndc": "50090-4741",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "210622",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "5MG/5ML",
"product_no": "001",
"approval_date": "Mar 13, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CETIRIZINE HYDROCHLORIDE",
"proprietary_name": "CHILDRENS ALLERGY RELIEF",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA210622",
"marketing_category": "ANDA",
"nonproprietary_name": "cetirizine hydrochloride",
"start_marketing_date": "20190313",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code R06AE.
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