Home NDC 0220-4600 SCUTELLARIA LATERIFLORA
Product NDC 0220-4600
11-digit product format 002204600
Labeler code 0220
Product ID 0220-4600_3a88b661-0b83-6225-e063-6394a90a18e7
Type HUMAN OTC DRUG
Nonproprietary name SCUTELLARIA LATERIFLORA WHOLE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance SCUTELLARIA LATERIFLORA WHOLE
Active strength 200 [kp_C]/200[kp_C]
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 SCUTELLARIA LATERIFLORA
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SCUTELLARIA LATERIFLORA WHOLE 200 [kp_C]/200[kp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7BP4DH5PDC 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 0220-4600-41 SCUTELLARIA LATERIFLORA 200 [kp_C] in 1 TUBE PELLET 200 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 Marketing start Sample Exclude flag Status 0220-4600-41 00220460041 200 [kp_C] in 1 TUBE (0220-4600-41) 2025-01-01 No No Current