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United States · US · US:0363-7570_44e3b064-1d55-f8e8-e063-6294a90a3559
Walgreens DAY and NIGHT PACK
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWALGREEN CO
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1103637570081 KIT in 1 KIT (0363-7570-08) * 118 mL in 1 BOTTLE (0363-7572-04) * 118 mL in 1 BOTTLE (0363-7571-04)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"34952272-1f9e-c642-e063-6394a90ae2bd": {
"match": "brand_token",
"title": "WALGREENS SCALP ITCH RELIEF (HYDROCORTISONE) LIQUID [WALGREENS]",
"spl_version": "2",
"published_date": "2026-06-01"
}
},
"productid": "0363-7570_44e3b064-1d55-f8e8-e063-6294a90a3559",
"productndc": "0363-7570",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Walgreens DAY and NIGHT PACK",
"active_ingred_unit": null,
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Dextromethorphan HBr, Guaifenesin, Chlorpheniramine maleate",
"start_marketing_date": "20200413",
"active_numerator_strength": null
}Access this data programmatically
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