Home NDC 0220-3638 Natrum sulphuricum
Product NDC 0220-3638
11-digit product format 002203638
Labeler code 0220
Product ID 0220-3638_f19d3bef-676b-0c62-e053-2995a90affa5
Type HUMAN OTC DRUG
Nonproprietary name SODIUM SULFATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance SODIUM SULFATE
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 Natrum sulphuricum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM SULFATE 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 0YPR65R21J 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 0220-3638-41 Natrum sulphuricum 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 0220-3638 NATRUM SULPHURICUM (SODIUM SULFATE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230107_86475307-ddef-1f41-e053-2991aa0a11f1.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 0220-3638-41 00220363841 15 [hp_C] in 1 TUBE (0220-3638-41) 1983-03-03 0000-00-00 No No Current