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United States · US · US:83819-306_8610aba0-cfc8-49b6-90e0-ec4e4dfd9aa7
dermveda PSORIASIS AND SEBORRHEIC DERMATITIS
UNIISPLATC D10AB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCelcius Corp.
CountryUS (United States)
ATC codeD10AB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11838193060260 mL in 1 CONTAINER (83819-306-02)
Annotations
UNII (FDA Substance ID)
W5488JUO8U
CURCUMA LONGA WHOLE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "W5488JUO8U",
"rxcui": null,
"inchikey": null,
"display_name": "CURCUMA LONGA WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"f43bc300-50bf-421a-81f8-1da7fc829cd0": {
"match": "brand_token",
"title": "DERMVEDA ULTRA FOLLICULITIS TREATMENT (SULFUR, CURCUMA LONGA) CREAM [CELCIUS CORP.]",
"spl_version": "1",
"published_date": "2026-06-01"
}
},
"productid": "83819-306_8610aba0-cfc8-49b6-90e0-ec4e4dfd9aa7",
"productndc": "83819-306",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CURCUMA LONGA WHOLE; SULFUR",
"proprietary_name": "dermveda PSORIASIS AND SEBORRHEIC DERMATITIS",
"active_ingred_unit": "[hp_C]/60mL; [hp_X]/60mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Sulfur, Curcuma Longa",
"start_marketing_date": "20240501",
"active_numerator_strength": "10; 10"
}Related drugs
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