Home NDC 85818-006-01 Dr.Johnes Arnica Bruise Arnica Montana 1X HPUS (7%)
Product NDC 85818-006
Requested package NDC 85818-006-01
11-digit product format 858180006
Labeler code 85818
Product ID 85818-006_bcd5501e-49bb-4b5d-abdc-5cc7e86f9306
Type HUMAN OTC DRUG
Nonproprietary name Arnica Montana 1X HPUS (7%)
Dosage form CREAM
Route TOPICAL
Labeler Dr.Johnes LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-07-19
Substance ARNICA MONTANA
Active strength 7 mg/100g
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Dr.Johnes Arnica Bruise Arnica Montana 1X HPUS (7%)
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 7 mg/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O80TY208ZW 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 Status 85818-006-01 85818000601 100 g in 1 JAR (85818-006-01) 100 g 2025-07-19 0 Current