Pancreas Equisetum

Product NDC
48951-8002
11-digit product format
489518002
Labeler code
48951
Product ID
48951-8002_49ef4761-1a55-e16b-e063-6394a90a6297
Type
HUMAN OTC DRUG
Nonproprietary name
Pancreas Equisetum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
EQUISETUM ARVENSE TOP; QUERCUS ROBUR WHOLE; SUS SCROFA PANCREAS
Active strength
6; 5; 5 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pancreas Equisetum
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SUS SCROFA PANCREAS6 [hp_X]/mL
QUERCUS ROBUR WHOLE5 [hp_X]/mL
EQUISETUM ARVENSE TOP5 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9Y3J3362RYInternal UNII lookup
R7QMG0BT2WInternal UNII lookup
1DP6Y6B65ZInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
7920248d-bb69-4403-8b79-1a60c4c70db6Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8002-1Pancreas Equisetum1 mL in 1 AMPULELIQUID16
48951-8002-1Pancreas Equisetum10 in 1 BOXLIQUID106

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1
QUERCUS ROBUR WHOLEACTIVE INGREDIENTR7QMG0BT2WPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA PANCREASACTIVE INGREDIENT9Y3J3362RYPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1
QUERCUS ROBUR WHOLEACTIVE MOIETYR7QMG0BT2WPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA PANCREASACTIVE MOIETY9Y3J3362RYPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8002PANCREAS EQUISETUM LIQUID [URIEL PHARMACY INC.]5Current NDC, Legacy NDC, 2 package rows20250129_7920248d-bb69-4403-8b79-1a60c4c70db6.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
Pancreas EquisetumPANCREAS EQUISETUMUriel Pharmacy Inc.7920248d-bb69-4403-8b79-1a60c4c70db62026-02-03WarningsExact identifier
ndc (product): 48951-8002

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8002-14895180020110 AMPULE in 1 BOX (48951-8002-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent