Home NDC 83819-987 dermveda ULTRA BALANITIS RELIEF
Product NDC 83819-987
11-digit product format 838190987
Labeler code 83819
Product ID 83819-987_7659bda6-ed60-4559-a80a-96d5d030fd1d
Type HUMAN OTC DRUG
Nonproprietary name Cardiospermum, Curcuma Longa
Dosage form SOLUTION
Route TOPICAL
Labeler Celcius Corp.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-08-11
Substance CARDIOSPERMUM HALICACABUM FLOWERING TOP; 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 BALANITIS RELIEF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARDIOSPERMUM HALICACABUM FLOWERING TOP 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 MZP2508BRR Internal UNII lookup 856YO1Z64F Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 83819-987-02 83819098702 60 mL in 1 JAR (83819-987-02) 60 ml 2026-08-11 No No Current