Natrum Sulphuratum

Product NDC
37662-1183
11-digit product format
376621183
Labeler code
37662
Product ID
37662-1183_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
1 [hp_Q]/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 SULFATE1 [hp_Q]/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
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
37662-1183-1Natrum Sulphuratum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-1183NATRUM SULPHURATUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 1 package rows20220805_e55f6111-c93f-26d0-e053-2995a90ae173.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-1183-13766211830110000 PELLET in 1 BOTTLE, GLASS (37662-1183-1) 10000 pellet2022-08-030000-00-00NoNoCurrent