Home NDC 43689-0035 Magnilife Eczema Care
Product NDC 43689-0035
11-digit product format 436890035
Labeler code 43689
Product ID 43689-0035_5681a398-bb4e-f076-e063-6294a90ae348
Type HUMAN OTC DRUG
Nonproprietary name SULFUR, GRAPHITE, DAPHNE MEZEREUM BARK, TOXICODENDRON PUBESCENS WHOLE
Dosage form CREAM
Route TOPICAL
Labeler The Magni Group, Inc.
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-09
Substance SULFUR; GRAPHITE; DAPHNE MEZEREUM BARK; TOXICODENDRON PUBESCENS WHOLE
Active strength 1; 3; 6; 6 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
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 Magnilife Eczema Care
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 1 [hp_X]/g GRAPHITE 3 [hp_X]/g DAPHNE MEZEREUM BARK 6 [hp_X]/g TOXICODENDRON PUBESCENS WHOLE 6 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 8 of 55 · 1,088 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 43689-0035-1 43689003501 1 JAR in 1 BOX, UNIT-DOSE (43689-0035-1) / 56 g in 1 JAR 1 jar 2026-07-09 No No Current