Home NDC 85248-026 REDCOOL Arnica Bruise
Product NDC 85248-026
11-digit product format 852480026
Labeler code 85248
Product ID 85248-026_5707c417-b73e-4bba-e063-6294a90a891e
Type HUMAN OTC DRUG
Nonproprietary name Arnica montana HPUS 7% Arnica Bruise
Dosage form CREAM
Route TOPICAL
Labeler Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-30
Substance ARNICA MONTANA
Active strength 7 g/100g
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 REDCOOL Arnica Bruise
Listing expiration 2027-12-31 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85248-026-01 REDCOOL Arnica Bruise 120 g in 1 BOTTLE CREAM 120 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 112 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85248-026-01 85248002601 120 g in 1 BOTTLE (85248-026-01) 120 g 2026-01-30 No No Current