Home NDC 76472-4098 Natrum Sulphuricum
Product NDC 76472-4098
11-digit product format 764724098
Labeler code 76472
Product ID 76472-4098_2ddc6261-f3c4-fd95-e063-6394a90a26a0
Type HUMAN OTC DRUG
Nonproprietary name SODIUM SULFATE
Dosage form PELLET
Route SUBLINGUAL
Labeler SEVENE USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-06-26
Substance SODIUM SULFATE
Active strength 6 [hp_X]/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 76472-4098-1 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76472-4098-1 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76472-4098-1 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Natrum Sulphuricum
Brand name suffix 6X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM SULFATE 6 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0YPR65R21J Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76472-4098-1 Natrum Sulphuricum6X 80 in 1 CYLINDER PELLET 80 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76472-4098 NATRUM SULPHURICUM 6X (SODIUM SULFATE) PELLET [SEVENE USA] 4 Current NDC, 1 package rows 20250213_ff0d6e73-5c50-daa2-e053-6294a90a293f.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 Units Marketing start Sample Exclude flag Status 76472-4098-1 76472409801 80 PELLET in 1 CYLINDER (76472-4098-1) 80 pellet 2023-06-26 No No Current