FDA.reportPublic FDA data

Natrum sulphuricum

Product NDC
0220-3643
Requested package NDC
0220-3643-41
11-digit product format
002203643
Labeler code
0220
Product ID
0220-3643_0a1fbdfd-54f3-cbfd-e063-6394a90a2db8
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
1 [hp_M]/[hp_M]
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
IngredientStrength
SODIUM SULFATE1 [hp_M]/[hp_M]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0YPR65R21JInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
86564f9d-36b5-39cb-e053-2991aa0a5007Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3643-412023-11-14C16284748780-1f386c649-a323-0266-e053-dadaa90a7c1aNatrum sulphuricum 1M
0220-3643-412023-01-30C16284748780-1f386c649-a323-0266-e053-dadaa90a7c1aNatrum sulphuricum 1M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3643-41Natrum sulphuricum1 [hp_M] in 1 TUBEPELLET12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3643NATRUM SULPHURICUM (SODIUM SULFATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231115_86564f9d-36b5-39cb-e053-2991aa0a5007.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Natrum sulphuricumSODIUM SULFATEBoiron86564f9d-36b5-39cb-e053-2991aa0a50072023-11-14Exact identifier
ndc (package): 0220-3643-41
ndc (product): 0220-3643
ndc11 (package): 00220364341

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3643-41002203643411 [hp_M] in 1 TUBE (0220-3643-41) 1983-03-030000-00-00NoNoCurrent