CANTHARIS

Product NDC
15631-0105
Requested package NDC
15631-0105-0
11-digit product format
156310105
Labeler code
15631
Product ID
15631-0105_caa1398e-ab39-4ae6-e053-2995a90a0c18
Type
HUMAN OTC DRUG
Nonproprietary name
CANTHARIS
Dosage form
PELLET
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-10-06
Substance
LYTTA VESICATORIA
Active strength
3 [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 packagepackage15631-010515631-0105-0EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LYTTA VESICATORIA3 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3Q034RO3BTInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
642a1b2d-05cf-4711-b121-487e62eabf62Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0105-0CANTHARIS100 in 1 PACKAGEPELLET1003
15631-0105-1CANTHARIS200 in 1 PACKAGEPELLET2003
15631-0105-2CANTHARIS400 in 1 PACKAGEPELLET4003
15631-0105-3CANTHARIS750 in 1 PACKAGEPELLET7503
15631-0105-4CANTHARIS2500 in 1 PACKAGEPELLET25003
15631-0105-5CANTHARIS12500 in 1 PACKAGEPELLET125003
15631-0105-6CANTHARIS500 in 1 PACKAGEPELLET5003
15631-0105-7CANTHARIS1000 in 1 PACKAGEPELLET10003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LYTTA VESICATORIAACTIVE INGREDIENT3Q034RO3BTCANTHARIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
LYTTA VESICATORIAACTIVE MOIETY3Q034RO3BTCANTHARIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554CANTHARIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0105CANTHARIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]3Current NDC, Legacy NDC, 8 package rows20210903_642a1b2d-05cf-4711-b121-487e62eabf62.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
CANTHARISCANTHARISRxhomeo Private Limited d.b.a. Rxhomeo, Inc642a1b2d-05cf-4711-b121-487e62eabf622021-09-02WarningsExact identifier
ndc (package): 15631-0105-0
ndc (product): 15631-0105
ndc11 (package): 15631010500

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
15631-0105-015631010500100 PELLET in 1 PACKAGE (15631-0105-0) 100 pellet2018-01-010000-00-00NoNoCurrent