Home NDC 84558-028 PUTRIZEN ARNICA BRUISE RELIEF Cream
Product NDC 84558-028
11-digit product format 845580028
Labeler code 84558
Product ID 84558-028_58a8064b-32a0-839b-e063-6394a90abb4a
Type HUMAN OTC DRUG
Nonproprietary name PUTRIZEN ARNICA BRUISE RELIEF Cream
Dosage form CREAM
Route TOPICAL
Labeler GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-10
Substance ARNICA MONTANA
Active strength 15 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 PUTRIZEN ARNICA BRUISE RELIEF Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 15 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.
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 84558-028-01 84558002801 120 g in 1 BOTTLE (84558-028-01) 120 g 2026-08-10 No No Current