Home NDC 0220-4975 THEA SINENSIS
Product NDC 0220-4975
11-digit product format 002204975
Labeler code 0220
Product ID 0220-4975_3a74a057-3055-0486-e063-6294a90a2d9d
Type HUMAN OTC DRUG
Nonproprietary name GREEN TEA LEAF
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance GREEN TEA LEAF
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base THEA SINENSIS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GREEN TEA LEAF 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 W2ZU1RY8B0 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 0220-4975-41 THEA SINENSIS 200 [kp_C] in 1 TUBE PELLET 200 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 0220-4975-41 00220497541 200 [kp_C] in 1 TUBE (0220-4975-41) 2025-01-01 No No Current