FDA.reportPublic FDA data

Spongia Ovi

Product NDC
48951-8203
Requested package NDC
48951-8203-2
11-digit product format
489518203
Labeler code
48951
Product ID
48951-8203_6e0dcb18-e8be-fb3c-e053-2991aa0a84d4
Type
HUMAN OTC DRUG
Nonproprietary name
Spongia Ovi
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SPONGIA OFFICINALIS SKELETON, ROASTED; CHELIDONIUM MAJUS; COLCHICUM AUTUMNALE WHOLE; CALCIUM CARBONATE; SUGARCANE
Active strength
1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-820348951-8203-2IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8203-2Spongia Ovi1350 in 1 BOTTLE, GLASSPELLET13503

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CALCIUM CARBONATEACTIVE INGREDIENTH0G9379FGKSPONGIA OVI PELLET [URIEL PHARMACY INC.]1
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNNSPONGIA OVI PELLET [URIEL PHARMACY INC.]1
COLCHICUM AUTUMNALE WHOLEACTIVE INGREDIENTW79255C628SPONGIA OVI PELLET [URIEL PHARMACY INC.]1
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE INGREDIENT1PIP394IIDSPONGIA OVI PELLET [URIEL PHARMACY INC.]1
SUGARCANEACTIVE INGREDIENT81H2R5AOH3SPONGIA OVI PELLET [URIEL PHARMACY INC.]1
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZBSPONGIA OVI PELLET [URIEL PHARMACY INC.]1
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNNSPONGIA OVI PELLET [URIEL PHARMACY INC.]1
COLCHICUM AUTUMNALE WHOLEACTIVE MOIETYW79255C628SPONGIA OVI PELLET [URIEL PHARMACY INC.]1
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE MOIETY1PIP394IIDSPONGIA OVI PELLET [URIEL PHARMACY INC.]1
SUGARCANEACTIVE MOIETY81H2R5AOH3SPONGIA OVI PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554SPONGIA OVI PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8203SPONGIA OVI PELLET [URIEL PHARMACY INC.]3Legacy NDC, 1 package rows20180607_f55584ee-55c9-4f33-99c1-f0d9f0ae581e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8203-2489518203021350 PELLET in 1 BOTTLE, GLASS (48951-8203-2) 1350 pellet2009-09-010000-00-00NoNoCurrent