Home NDC 0220-0750 Baryta carbonica
Product NDC 0220-0750
11-digit product format 002200750
Labeler code 0220
Product ID 0220-0750_09ba4b09-2087-2f85-e063-6394a90a0f12
Type HUMAN OTC DRUG
Nonproprietary name BARIUM CARBONATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance BARIUM CARBONATE
Active strength 15 [hp_C]/15[hp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Baryta carbonica
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BARIUM CARBONATE 15 [hp_C]/15[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 6P669D8HQ8 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-0750-41 Baryta carbonica 15 [hp_C] in 1 TUBE PELLET 15 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0750 BARYTA CARBONICA (BARIUM CARBONATE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231110_847567fd-73d2-79c6-e053-2a91aa0ac629.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 0220-0750-41 00220075041 15 [hp_C] in 1 TUBE (0220-0750-41) 1983-03-03 0000-00-00 No No Current