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United States · US · US:0363-0966_24740d5a-aba3-0bd4-e063-6394a90ab2ca
Walgreens Sunburn Relief
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWALGREEN COMPANY
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110363096615170 g in 1 TUBE (0363-0966-15)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"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": "0363-0966_24740d5a-aba3-0bd4-e063-6394a90ab2ca",
"productndc": "0363-0966",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "Walgreens Sunburn Relief",
"active_ingred_unit": "mg/g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Menthol",
"start_marketing_date": "20170911",
"active_numerator_strength": "5"
}Access this data programmatically
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