Ignatia Bryophyllum

Product NDC
48951-5068
11-digit product format
489515068
Labeler code
48951
Product ID
48951-5068_2c91179e-9a13-a931-e063-6394a90aa7d2
Type
HUMAN OTC DRUG
Nonproprietary name
Ignatia Bryophyllum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
KALANCHOE DAIGREMONTIANA LEAF; STRYCHNOS IGNATII SEED; SILVER; LACHESIS MUTA VENOM
Active strength
3; 4; 10; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
KALANCHOE DAIGREMONTIANA LEAF3 [hp_X]/mL
STRYCHNOS IGNATII SEED4 [hp_X]/mL
SILVER10 [hp_X]/mL
LACHESIS MUTA VENOM12 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L6X13JKL8OInternal UNII lookup
1NM3M2487KInternal UNII lookup
3M4G523W1GInternal UNII lookup
VSW71SS07IInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4e8711b9-5623-43aa-ad8e-1d6893c09999Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-5068-1Ignatia Bryophyllum1 mL in 1 AMPULELIQUID14
48951-5068-1Ignatia Bryophyllum10 in 1 BOXLIQUID104

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
KALANCHOE DAIGREMONTIANA LEAFACTIVE INGREDIENTL6X13JKL8OIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07IIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE INGREDIENT3M4G523W1GIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487KIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
KALANCHOE DAIGREMONTIANA LEAFACTIVE MOIETYL6X13JKL8OIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07IIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE MOIETY3M4G523W1GIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487KIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RIGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5068IGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20250127_4e8711b9-5623-43aa-ad8e-1d6893c09999.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
Ignatia BryophyllumIGNATIA BRYOPHYLLUMUriel Pharmacy Inc.4e8711b9-5623-43aa-ad8e-1d6893c099992025-01-25WarningsExact identifier
ndc (product): 48951-5068

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-5068-14895150680110 AMPULE in 1 BOX (48951-5068-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent