Home NDC 48951-3283 Carbo Betulae 20
Product NDC 48951-3283
11-digit product format 489513283
Labeler code 48951
Product ID 48951-3283_3c4499d0-d95c-d57b-e063-6294a90a9955
Type HUMAN OTC DRUG
Nonproprietary name Carbo Betulae 20
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ACTIVATED CHARCOAL
Active strength 20 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Carbo Betulae 20
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACTIVATED CHARCOAL 20 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2P3VWU3H10 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 48951-3283-3 Carbo Betulae 20 60 mL in 1 BOTTLE, DROPPER LIQUID 60 4
DailyMed Socrata Ingredients# 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 48951-3283-3 48951328303 60 mL in 1 BOTTLE, DROPPER (48951-3283-3) 60 ml 2009-09-01 No No Current