Home NDC 83819-606 dermveda ULTRA FOLLICULITIS TREATMENT
Product NDC 83819-606
11-digit product format 838190606
Labeler code 83819
Product ID 83819-606_00956a31-f8e0-4aab-816f-718a19f8a8e8
Type HUMAN OTC DRUG
Nonproprietary name Sulfur, Curcuma Longa
Dosage form CREAM
Route TOPICAL
Labeler Celcius Corp.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-05-27
Substance SULFUR; TURMERIC
Active strength 10; 10 [hp_X]/60mL; [hp_C]/60mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base dermveda ULTRA FOLLICULITIS TREATMENT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 10 [hp_X]/60mL TURMERIC 10 [hp_C]/60mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup 856YO1Z64F Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83819-606-02 83819060602 60 mL in 1 JAR (83819-606-02) 60 ml 2026-05-27 No No Current