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United States · US · US:83819-303_89301776-acad-4ddb-9fbd-8f8a89f002fc
Dermveda SHINGLES RELIEF
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
- ndc11838193030260 mL in 1 JAR (83819-303-02)
Annotations
UNII (FDA Substance ID)
70FD1KFU70
SULFUR
RxCUI 10223
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "70FD1KFU70",
"rxcui": "10223",
"inchikey": "JLQNHALFVCURHW-UHFFFAOYSA-N",
"display_name": "SULFUR",
"substance_type": "chemical",
"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": "83819-303_89301776-acad-4ddb-9fbd-8f8a89f002fc",
"productndc": "83819-303",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SULFUR; TURMERIC",
"proprietary_name": "Dermveda SHINGLES RELIEF",
"active_ingred_unit": "[hp_X]/60mL; [hp_C]/60mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Sulphur, Curcuma Longa",
"start_marketing_date": "20240918",
"active_numerator_strength": "10; 10"
}Related drugs
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