Home NDC 48951-7222 Melissa
Product NDC 48951-7222
11-digit product format 489517222
Labeler code 48951
Product ID 48951-7222_3eef31ef-39a4-3813-e063-6394a90a82af
Type HUMAN OTC DRUG
Nonproprietary name Melissa
Dosage form GEL
Route TOPICAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance MELISSA OFFICINALIS; ACONITUM NAPELLUS; TOXICODENDRON PUBESCENS LEAF; ATROPA BELLADONNA
Active strength 1; 30; 30; 30 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
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 Melissa
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MELISSA OFFICINALIS 1 [hp_X]/g ACONITUM NAPELLUS 30 [hp_X]/g TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/g ATROPA BELLADONNA 30 [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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-7222-1 Melissa 10 g in 1 TUBE GEL 10 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 48951-7222-1 48951722201 10 g in 1 TUBE (48951-7222-1) 10 g 2009-09-01 No No Current