FDA.reportPublic FDA data

Sulphur

Product NDC
37662-2317
11-digit product format
376622317
Labeler code
37662
Product ID
37662-2317_f208f88c-3c4e-f177-e053-2995a90aba01
Type
HUMAN OTC DRUG
Nonproprietary name
Sulphur
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-01-11
Substance
SULFUR
Active strength
200 [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
Sulphur
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR200 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii70FD1KFU70

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2317-1Sulphur200 in 1 VIAL, GLASSPELLET2001
37662-2317-2Sulphur500 in 1 VIAL, GLASSPELLET5001
37662-2317-3Sulphur3000 in 1 BOTTLE, GLASSPELLET30001
37662-2317-4Sulphur10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2317SULPHUR PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 4 package rows20230112_f208f88c-3c4d-f177-e053-2995a90aba01.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-2317-137662231701200 PELLET in 1 VIAL, GLASS (37662-2317-1) 200 pellet2023-01-110000-00-00NoNoCurrent
37662-2317-237662231702500 PELLET in 1 VIAL, GLASS (37662-2317-2) 500 pellet2023-01-110000-00-00NoNoCurrent
37662-2317-3376622317033000 PELLET in 1 BOTTLE, GLASS (37662-2317-3) 3000 pellet2023-01-110000-00-00NoNoCurrent
37662-2317-43766223170410000 PELLET in 1 BOTTLE, GLASS (37662-2317-4) 10000 pellet2023-01-110000-00-00NoNoCurrent