Home NDC 48951-2163 Bryophyllum Argento culta 3X
Product NDC 48951-2163
11-digit product format 489512163
Labeler code 48951
Product ID 48951-2163_4d7a929d-cbca-6706-e063-6294a90a5e06
Type HUMAN OTC DRUG
Nonproprietary name Bryophyllum Argento culta 3x
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance SILVER; KALANCHOE DAIGREMONTIANA LEAF
Active strength 3; 3 [hp_X]/mL; [hp_X]/mL
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 Bryophyllum Argento culta 3X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILVER 3 [hp_X]/mL KALANCHOE DAIGREMONTIANA LEAF 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3M4G523W1G Internal UNII lookup L6X13JKL8O 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 48951-2163-3 Bryophyllum Argento culta 3X 60 mL in 1 BOTTLE, DROPPER LIQUID 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 48951-2163-3 48951216303 60 mL in 1 BOTTLE, DROPPER (48951-2163-3) 60 ml 2009-09-01 No No Current