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United States · US · US:11673-877_17b7ffd1-5422-4b0e-9fec-e7e93fe97f4b
Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough
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
- ndc1111673877551 KIT in 1 CARTON (11673-877-55) * 1 POWDER, FOR SOLUTION in 1 PACKET (82442-122-00) * 1 POWDER, FOR SOLUTION in 1 PACKET (82442-964-00)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"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": "11673-877_17b7ffd1-5422-4b0e-9fec-e7e93fe97f4b",
"productndc": "11673-877",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough",
"active_ingred_unit": null,
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, diphenhydramine hydrochloride",
"start_marketing_date": "20210716",
"active_numerator_strength": null
}Access this data programmatically
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