Home NDC 62106-1170 UNDA 600
Product NDC 62106-1170
11-digit product format 621061170
Labeler code 62106
Product ID 62106-1170_ed12a71d-e8f3-b336-e053-2a95a90a4f09
Type HUMAN OTC DRUG
Nonproprietary name Berberis vulgaris, Rheum, Rhus toxicodendron
Dosage form LIQUID
Route ORAL
Labeler Seroyal USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-05-05
Substance RHEUM OFFICINALE ROOT; BERBERIS VULGARIS ROOT BARK; TOXICODENDRON PUBESCENS SHOOT
Active strength 6; 6; 6 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL
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 UNDA 600
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RHEUM OFFICINALE ROOT 6 [hp_X]/20mL BERBERIS VULGARIS ROOT BARK 6 [hp_X]/20mL TOXICODENDRON PUBESCENS SHOOT 6 [hp_X]/20mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination A47JP5ZG9M Internal UNII lookup 1TH8Q20J0U Internal UNII lookup 46PYZ1F82M 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 62106-1170-8 UNDA 600 1 in 1 CARTON LIQUID 1 3 62106-1170-8 UNDA 600 20 mL in 1 BOTTLE, GLASS LIQUID 20 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62106-1170 UNDA 600 (BERBERIS VULGARIS, RHEUM, RHUS TOXICODENDRON) LIQUID [SEROYAL USA] 3 Current NDC, Legacy NDC, 2 package rows 20221111_4d505bd6-2819-6c7f-e054-00144ff88e88.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 Marketing start Marketing end Sample Exclude flag Status 62106-1170-8 62106117008 1 BOTTLE, GLASS in 1 CARTON (62106-1170-8) / 20 mL in 1 BOTTLE, GLASS 2017-05-05 0000-00-00 No No Current