Home NDC 48951-1400 Arnica Nettle
Product NDC 48951-1400
11-digit product format 489511400
Labeler code 48951
Product ID 48951-1400_4575a910-3ae4-ca6c-e063-6294a90a76e0
Type HUMAN OTC DRUG
Nonproprietary name Arnica Nettle
Dosage form OINTMENT
Route TOPICAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ARNICA MONTANA FLOWER; URTICA URENS
Active strength 1; 1 [hp_X]/g; [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Arnica Nettle
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength URTICA URENS 1 [hp_X]/g ARNICA MONTANA FLOWER 1 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination IHN2NQ5OF9 Internal UNII lookup OZ0E5Y15PZ 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 48951-1400-2 Arnica Nettle 30 g in 1 TUBE OINTMENT 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1400 ARNICA NETTLE OINTMENT [URIEL PHARMACY, INC] 1 Current NDC, 1 package rows 20250309_2eae3874-3893-08d0-e063-6294a90ac42e.zip
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 48951-1400-2 48951140002 30 g in 1 TUBE (48951-1400-2) 30 g 2009-09-01 No No Current