FDA.reportPublic FDA data

BM Rhus Tox

Product NDC
85816-6023
Requested package NDC
85816-6023-2
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

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
IngredientStrength
CINNAMON1 [hp_X]/g
ARNICA MONTANA1 [hp_X]/g
BELLIS PERENNIS1 [hp_X]/g
BRYONIA ALBA ROOT7 [hp_X]/g
CAMPHOR (NATURAL)1 [hp_X]/g
TURMERIC1 [hp_X]/g
COLCHICUM AUTUMNALE BULB6 [hp_X]/g
TOXICODENDRON PUBESCENS LEAF6 [hp_X]/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5S29HWU6QBInternal UNII lookup
O80TY208ZWInternal UNII lookup
2HU33I03UYInternal UNII lookup
T7J046YI2BInternal UNII lookup
N20HL7Q941Internal UNII lookup
856YO1Z64FInternal UNII lookup
993QHL78E6Internal UNII lookup
6IO182RP7AInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3890f0d6-0f02-2266-e063-6394a90ae2bcAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-6023-1BM Rhus Tox40 g in 1 JAROINTMENT404
85816-6023-2BM Rhus Tox40 g in 1 TUBEOINTMENT404

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BM Rhus ToxRHUS TOXBM Private Limited3890f0d6-0f02-2266-e063-6394a90ae2bc2026-02-12WarningsExact identifier
ndc (package): 85816-6023-2
ndc (product): 85816-6023
ndc11 (package): 85816602302

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85816-6023-28581660230240 g in 1 TUBE (85816-6023-2) 40 g2025-10-10NoNoCurrent