Home NDC 48951-1408 Amber Amethyst
Product NDC 48951-1408
11-digit product format 489511408
Labeler code 48951
Product ID 48951-1408_4837e805-a778-c1fa-e063-6294a90ae9c4
Type HUMAN OTC DRUG
Nonproprietary name Amber Amethyst
Dosage form OINTMENT
Route TOPICAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance AMBER; EQUISETUM ARVENSE WHOLE; HORSE CHESTNUT; SILICON DIOXIDE
Active strength 3; 2; 2; 6 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Amber Amethyst
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HORSE CHESTNUT 3 [hp_X]/g AMBER 2 [hp_X]/g EQUISETUM ARVENSE WHOLE 2 [hp_X]/g SILICON DIOXIDE 6 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 48951-1408-5 Amber Amethyst 60 g in 1 TUBE OINTMENT 60 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 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 48951-1408-5 48951140805 60 g in 1 TUBE (48951-1408-5) 60 g 2009-09-01 No No Current