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

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
IngredientStrength
SODIUM SULFATE6 [hp_X]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0YPR65R21J

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-4098-1Natrum Sulphuricum6X80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-4098NATRUM SULPHURICUM 6X (SODIUM SULFATE) PELLET [SEVENE USA]4Current NDC, 1 package rows20250213_ff0d6e73-5c50-daa2-e053-6294a90a293f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76472-4098-17647240980180 PELLET in 1 CYLINDER (76472-4098-1) 80 pellet2023-06-26NoNoCurrent