Home NDC 85398-005-01 Arnica Bruise Cream
Product NDC 85398-005
Requested package NDC 85398-005-01
11-digit product format 853980005
Labeler code 85398
Product ID 85398-005_4c06d625-72cc-1cb4-e063-6294a90aff24
Type HUMAN OTC DRUG
Nonproprietary name Arnica Montana
Dosage form CREAM
Route TOPICAL
Labeler Beautivity LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-05-30
Substance ARNICA MONTANA
Active strength 1 [hp_X]/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Arnica Bruise Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 1 [hp_X]/1
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85398-005-01 Arnica Bruise Cream 1 in 1 JAR CREAM 1 2
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 85398-005-01 85398000501 1 CREAM in 1 JAR (85398-005-01) 1 cream 2025-05-30 No No Current