Home NDC 83818-025 SupreH Arnica Bruise Cream
Product NDC 83818-025
11-digit product format 838180025
Labeler code 83818
Product ID 83818-025_3e41fc0e-54c4-2622-e063-6294a90a13c9
Type HUMAN OTC DRUG
Nonproprietary name SupreH ARNICA REMEDY PLUS BRUISE Cream
Dosage form CREAM
Route TOPICAL
Labeler Shenzhen Xinxin Yunhai Technology Co., Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-08
Substance ARNICA MONTANA
Active strength 7 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
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 SupreH Arnica Bruise Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 7 g/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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83818-025-01 SupreH Arnica Bruise Cream 114 g in 1 JAR CREAM 114 1
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 109 of 152 · 3,029 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83818-025-01 83818002501 114 g in 1 JAR (83818-025-01) 114 g 2025-09-08 No No Current