EUPHRASIA OFFICINALIS

Product NDC
15631-0184
Requested package NDC
15631-0184-0
11-digit product format
156310184
Labeler code
15631
Product ID
15631-0184_cdda036a-8e4c-1a19-e053-2995a90a834a
Type
HUMAN OTC DRUG
Nonproprietary name
EUPHRASIA OFFICINALIS
Dosage form
PELLET
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-10-02
Substance
EUPHRASIA STRICTA
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 packagepackage15631-018415631-0184-0EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EUPHRASIA STRICTA1 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
C9642I91WLInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
1cf52c36-a405-40a8-a492-20df572aedf2Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0184-0EUPHRASIA OFFICINALIS100 in 1 PACKAGEPELLET1003
15631-0184-1EUPHRASIA OFFICINALIS200 in 1 PACKAGEPELLET2003
15631-0184-2EUPHRASIA OFFICINALIS400 in 1 PACKAGEPELLET4003
15631-0184-3EUPHRASIA OFFICINALIS750 in 1 PACKAGEPELLET7503
15631-0184-4EUPHRASIA OFFICINALIS2500 in 1 PACKAGEPELLET25003
15631-0184-5EUPHRASIA OFFICINALIS12500 in 1 PACKAGEPELLET125003
15631-0184-6EUPHRASIA OFFICINALIS500 in 1 PACKAGEPELLET5003
15631-0184-7EUPHRASIA OFFICINALIS1000 in 1 PACKAGEPELLET10003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EUPHRASIA STRICTAACTIVE INGREDIENTC9642I91WLEUPHRASIA OFFICINALIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
EUPHRASIA STRICTAACTIVE MOIETYC9642I91WLEUPHRASIA OFFICINALIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554EUPHRASIA OFFICINALIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0184EUPHRASIA OFFICINALIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]3Current NDC, Legacy NDC, 8 package rows20211009_1cf52c36-a405-40a8-a492-20df572aedf2.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
EUPHRASIA OFFICINALISEUPHRASIA OFFICINALISRxhomeo Private Limited d.b.a. Rxhomeo, Inc1cf52c36-a405-40a8-a492-20df572aedf22021-10-08WarningsExact identifier
ndc (package): 15631-0184-0
ndc (product): 15631-0184
ndc11 (package): 15631018400

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
15631-0184-015631018400100 PELLET in 1 PACKAGE (15631-0184-0) 100 pellet2018-01-010000-00-00NoNoCurrent