FDA.reportPublic FDA data

Natrum Sulphuratum

Product NDC
37662-1178
11-digit product format
376621178
Labeler code
37662
Product ID
37662-1178_e55f6111-c940-26d0-e053-2995a90ae173
Type
HUMAN OTC DRUG
Nonproprietary name
Natrum Sulphuratum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-08-03
Substance
SODIUM SULFATE
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
Natrum Sulphuratum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM SULFATE30 [hp_C]/1

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
e55f6111-c93f-26d0-e053-2995a90ae173Available 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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-1178-1Natrum Sulphuratum80 in 1 VIAL, GLASSPELLET801
37662-1178-2Natrum Sulphuratum200 in 1 VIAL, GLASSPELLET2001
37662-1178-3Natrum Sulphuratum1200 in 1 BOTTLE, GLASSPELLET12001
37662-1178-4Natrum Sulphuratum4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-1178NATRUM SULPHURATUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 4 package rows20220805_e55f6111-c93f-26d0-e053-2995a90ae173.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 SulphuratumNATRUM SULPHURATUMHahnemann Laboratories, INC.e55f6111-c93f-26d0-e053-2995a90ae1732022-08-03Exact identifier
ndc (product): 37662-1178

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-1178-13766211780180 PELLET in 1 VIAL, GLASS (37662-1178-1) 80 pellet2022-08-030000-00-00NoNoCurrent
37662-1178-237662117802200 PELLET in 1 VIAL, GLASS (37662-1178-2) 200 pellet2022-08-030000-00-00NoNoCurrent
37662-1178-3376621178031200 PELLET in 1 BOTTLE, GLASS (37662-1178-3) 1200 pellet2022-08-030000-00-00NoNoCurrent
37662-1178-4376621178044000 PELLET in 1 BOTTLE, GLASS (37662-1178-4) 4000 pellet2022-08-030000-00-00NoNoCurrent