Home NDC 71919-829 Antimonium tartaricum
Product NDC 71919-829
11-digit product format 719190829
Labeler code 71919
Product ID 71919-829_3e89179f-2598-bca0-e063-6394a90a5b07
Type HUMAN OTC DRUG
Nonproprietary name ANTIMONY POTASSIUM TARTRATE
Dosage form PELLET
Route ORAL
Labeler Washington Homeopathic Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-09-11
Substance ANTIMONY POTASSIUM TARTRATE
Active strength 30 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Antimonium tartaricum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANTIMONY POTASSIUM TARTRATE 30 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination DL6OZ476V3 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 71919-829-05 Antimonium tartaricum 900 in 1 VIAL, GLASS PELLET 900 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 71919-829-05 71919082905 900 PELLET in 1 VIAL, GLASS (71919-829-05) 900 pellet 2025-09-11 No No Current