Home NDC 87681-003 RAVYNDRA Arnica Bruise Cream
Product NDC 87681-003
11-digit product format 876810003
Labeler code 87681
Product ID 87681-003_532eb266-93bf-6923-e063-6294a90ae329
Type HUMAN OTC DRUG
Nonproprietary name ARNICA MONTANA
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Xinhongda Trading Service Co., Ltd.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-06-01
Substance ARNICA MONTANA
Active strength 1 [hp_X]/7mL
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 RAVYNDRA Arnica Bruise Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 1 [hp_X]/7mL
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# 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 87681-003-01 87681000301 1 BOTTLE in 1 BOX (87681-003-01) / 100 mL in 1 BOTTLE 1 bottle 2026-06-01 No No Current