SULPHUR

Product NDC
15631-0420
Requested package NDC
15631-0420-2
11-digit product format
156310420
Labeler code
15631
Product ID
15631-0420_ca3d3f46-aec7-3b74-e053-2a95a90a2f07
Type
HUMAN OTC DRUG
Nonproprietary name
SULPHUR
Dosage form
PELLET
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-11-03
Substance
SULFUR
Active strength
1 [hp_X]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage15631-042015631-0420-2EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

Additional Listing Data#

Finished product
Yes
Brand name base
SULPHUR
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR1 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
70FD1KFU70Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
61a36a56-4e62-4721-81fb-ee8dcd08b4d8Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0420-0SULPHUR100 in 1 VIAL, SINGLE-DOSEPELLET1003
15631-0420-1SULPHUR200 in 1 PACKAGEPELLET2003
15631-0420-2SULPHUR400 in 1 PACKAGEPELLET4003
15631-0420-3SULPHUR750 in 1 PACKAGEPELLET7503
15631-0420-4SULPHUR2500 in 1 PACKAGEPELLET25003
15631-0420-5SULPHUR12500 in 1 PACKAGEPELLET125003
15631-0420-6SULPHUR500 in 1 PACKAGEPELLET5003
15631-0420-7SULPHUR1000 in 1 PACKAGEPELLET10003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SULFURACTIVE INGREDIENT70FD1KFU70SULPHUR PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
SULFURACTIVE MOIETY70FD1KFU70SULPHUR PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554SULPHUR PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0420SULPHUR PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]3Current NDC, Legacy NDC, 8 package rows20210903_61a36a56-4e62-4721-81fb-ee8dcd08b4d8.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
SULPHURSULPHURRxhomeo Private Limited d.b.a. Rxhomeo, Inc61a36a56-4e62-4721-81fb-ee8dcd08b4d82021-09-02WarningsExact identifier
ndc (package): 15631-0420-2
ndc (product): 15631-0420
ndc11 (package): 15631042002

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
15631-0420-215631042002400 PELLET in 1 PACKAGE (15631-0420-2) 400 pellet2018-01-010000-00-00NoNoCurrent