Home NDC 0220-9103 Bone Pain Relief
Product NDC 0220-9103
11-digit product format 002209103
Labeler code 0220
Product ID 0220-9103_52419c5d-bf47-67ca-e063-6294a90a8fe0
Type HUMAN OTC DRUG
Nonproprietary name COMFREY ROOT, TRIBASIC CALCIUM PHOSPHATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-02-01
Substance COMFREY ROOT; TRIBASIC CALCIUM PHOSPHATE
Active strength 6; 30 [hp_C]/1; [hp_C]/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Bone Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRIBASIC CALCIUM PHOSPHATE 30 [hp_C]/1 COMFREY ROOT 6 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 91D9GV0Z28 Internal UNII lookup M9VVZ08EKQ Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-9103-43 Bone Pain Relief 3 in 1 CARTON PELLET 3 1 0220-9103-43 Bone Pain Relief 80 in 1 TUBE PELLET 80 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 0220-9103-43 00220910343 3 TUBE in 1 CARTON (0220-9103-43) / 80 PELLET in 1 TUBE 3 tube 2026-02-01 No No Current