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United States · US · US:11673-282_b49993f2-3596-46fa-bb42-c4bf31cdf5da
Daytime Nighttime Sinus Relief
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1111673282091 KIT in 1 CARTON (11673-282-09) * 12 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"4779288a-9850-8490-e063-6394a90abe51": {
"match": "brand_token",
"title": "DAYTIME NIGHTTIME (ACETAMINOPHEN DEXTROMETHORPHAN HBR, ACETAMINOPHEN DEXTROMETHORPHAN HBR TRIPROLIDINE HCL) KIT [TARGET CORPORATION]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "11673-282_b49993f2-3596-46fa-bb42-c4bf31cdf5da",
"productndc": "11673-282",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Daytime Nighttime Sinus Relief",
"active_ingred_unit": null,
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Acetaminophen, Diphenhydramine HCl, Guaifenesin, Phenylephrine HCl",
"start_marketing_date": "20240415",
"active_numerator_strength": null
}Access this data programmatically
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