PHOSPHORUS

Product NDC
15631-0336
Requested package NDC
15631-0336-1
11-digit product format
156310336
Labeler code
15631
Product ID
15631-0336_ca7b6768-4d86-1c6d-e053-2995a90a2319
Type
HUMAN OTC DRUG
Nonproprietary name
PHOSPHORUS
Dosage form
PELLET
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-09-12
Substance
PHOSPHORUS
Active strength
4 [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 packagepackage15631-033615631-0336-1EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHOSPHORUS4 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
27YLU75U4WInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
21fa8f76-af69-4812-b291-a6bdeffbfd00Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0336-0PHOSPHORUS100 in 1 PACKAGEPELLET1004
15631-0336-1PHOSPHORUS200 in 1 PACKAGEPELLET2004
15631-0336-2PHOSPHORUS400 in 1 PACKAGEPELLET4004
15631-0336-3PHOSPHORUS750 in 1 PACKAGEPELLET7504
15631-0336-4PHOSPHORUS2500 in 1 PACKAGEPELLET25004
15631-0336-5PHOSPHORUS12500 in 1 PACKAGEPELLET125004
15631-0336-6PHOSPHORUS500 in 1 PACKAGEPELLET5004
15631-0336-7PHOSPHORUS1000 in 1 PACKAGEPELLET10004

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PHOSPHORUSACTIVE INGREDIENT27YLU75U4WPHOSPHORUS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]2
PHOSPHORUSACTIVE MOIETY27YLU75U4WPHOSPHORUS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]2
SUCROSEINACTIVE INGREDIENTC151H8M554PHOSPHORUS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0336PHOSPHORUS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]4Current NDC, Legacy NDC, 8 package rows20210903_21fa8f76-af69-4812-b291-a6bdeffbfd00.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
PHOSPHORUSPHOSPHORUSRxhomeo Private Limited d.b.a. Rxhomeo, Inc21fa8f76-af69-4812-b291-a6bdeffbfd002021-09-02WarningsExact identifier
ndc (package): 15631-0336-1
ndc (product): 15631-0336
ndc11 (package): 15631033601

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
15631-0336-115631033601200 PELLET in 1 PACKAGE (15631-0336-1) 200 pellet2018-01-010000-00-00NoNoCurrent