FDA.reportPublic FDA data

Cocculus Conium

Product NDC
48951-3109
11-digit product format
489513109
Labeler code
48951
Product ID
48951-3109_2b617508-1882-a05a-e063-6294a90a6f18
Type
HUMAN OTC DRUG
Nonproprietary name
Cocculus Conium
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
AMBERGRIS; ANAMIRTA COCCULUS WHOLE; CONIUM MACULATUM ROOT; LIQUID PETROLEUM
Active strength
7; 4; 4; 9 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANAMIRTA COCCULUS WHOLE7 [hp_X]/1
CONIUM MACULATUM ROOT4 [hp_X]/1
AMBERGRIS4 [hp_X]/1
LIQUID PETROLEUM9 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8O4P2U3QO2Internal UNII lookup
TTE3RU7P5PInternal UNII lookup
XTC0D02P6CInternal UNII lookup
6ZAE7X688JInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
031fe9cd-8fc6-4004-a99b-83ae066d52a7Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3109-2Cocculus Conium1350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMBERGRISACTIVE INGREDIENTXTC0D02P6CCOCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
ANAMIRTA COCCULUS WHOLEACTIVE INGREDIENT8O4P2U3QO2COCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
CONIUM MACULATUM ROOTACTIVE INGREDIENTTTE3RU7P5PCOCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
LIQUID PETROLEUMACTIVE INGREDIENT6ZAE7X688JCOCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
AMBERGRISACTIVE MOIETYXTC0D02P6CCOCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
ANAMIRTA COCCULUS WHOLEACTIVE MOIETY8O4P2U3QO2COCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
CONIUM MACULATUM ROOTACTIVE MOIETYTTE3RU7P5PCOCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
LIQUID PETROLEUMACTIVE MOIETY6ZAE7X688JCOCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554COCCULUS CONIUM PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3109COCCULUS CONIUM PELLET [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 1 package rows20250112_031fe9cd-8fc6-4004-a99b-83ae066d52a7.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
Cocculus ConiumCOCCULUS CONIUMUriel Pharmacy Inc.031fe9cd-8fc6-4004-a99b-83ae066d52a72025-01-10WarningsExact identifier
ndc (product): 48951-3109

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3109-2489513109021350 PELLET in 1 BOTTLE, GLASS (48951-3109-2) 1350 pellet2009-09-010000-00-00NoNoCurrent