Home NDC 85816-6023 BM Rhus Tox
Product NDC 85816-6023
11-digit product format 858166023
Labeler code 85816
Product ID 85816-6023_4aa04a61-ac81-e9d1-e063-6394a90a2902
Type HUMAN OTC DRUG
Nonproprietary name Rhus Tox
Dosage form OINTMENT
Route TOPICAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance CINNAMON; ARNICA MONTANA; BELLIS PERENNIS; BRYONIA ALBA ROOT; CAMPHOR (NATURAL); TURMERIC; COLCHICUM AUTUMNALE BULB; TOXICODENDRON PUBESCENS LEAF
Active strength 1; 1; 1; 7; 1; 1; 6; 6 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 85816-6023 85816-6023-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 Rhus Tox
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CINNAMON 1 [hp_X]/g ARNICA MONTANA 1 [hp_X]/g BELLIS PERENNIS 1 [hp_X]/g BRYONIA ALBA ROOT 7 [hp_X]/g CAMPHOR (NATURAL) 1 [hp_X]/g TURMERIC 1 [hp_X]/g COLCHICUM AUTUMNALE BULB 6 [hp_X]/g TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 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 85816-6023-1 BM Rhus Tox 40 g in 1 JAR OINTMENT 40 4 85816-6023-2 BM Rhus Tox 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 85816-6023-1 85816602301 40 g in 1 JAR (85816-6023-1) 40 g 2015-01-01 No No Current 85816-6023-2 85816602302 40 g in 1 TUBE (85816-6023-2) 40 g 2025-10-10 No No Current