Home NDC 85816-6022-2 BM Eczema
Product NDC 85816-6022
Requested package NDC 85816-6022-2
11-digit product format 858166022
Labeler code 85816
Product ID 85816-6022_4aa03044-7ad2-45b6-e063-6394a90aef7d
Type HUMAN OTC DRUG
Nonproprietary name Calendula, Echinacea, Graphite, Sulfur
Dosage form OINTMENT
Route TOPICAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance ECHINACEA, UNSPECIFIED; GRAPHITE; CALENDULA OFFICINALIS FLOWERING TOP; SULFUR
Active strength 1; 2; 1; 4 [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 BM Eczema
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA, UNSPECIFIED 1 [hp_X]/g GRAPHITE 2 [hp_X]/g CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/g SULFUR 4 [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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-6022-1 BM Eczema 40 g in 1 JAR OINTMENT 40 4 85816-6022-2 BM Eczema 40 g in 1 TUBE OINTMENT 40 4
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 85816-6022-2 85816602202 40 g in 1 TUBE (85816-6022-2) 40 g 2025-10-10 No No Current