Lachesis Belladonna

Product NDC
48951-6012
11-digit product format
489516012
Labeler code
48951
Product ID
48951-6012_2b24df98-1d29-5f7b-e063-6294a90a423a
Type
HUMAN OTC DRUG
Nonproprietary name
Lachesis Belladonna
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ATROPA BELLADONNA; CALCIUM SULFIDE; LACHESIS MUTA VENOM; MERCURIALIS PERENNIS
Active strength
4; 7; 12; 6 [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

Additional Listing Data#

Finished product
Yes
Brand name base
Lachesis Belladonna
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ATROPA BELLADONNA4 [hp_X]/mL
MERCURIALIS PERENNIS7 [hp_X]/mL
CALCIUM SULFIDE12 [hp_X]/mL
LACHESIS MUTA VENOM6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
WQZ3G9PF0HInternal UNII lookup
Q35465A1MAInternal UNII lookup
1MBW07J51QInternal 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
c617a849-5043-43cd-974f-2f0d664fd468Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-6012-1Lachesis Belladonna10 in 1 BOXLIQUID106
48951-6012-1Lachesis Belladonna1 mL in 1 AMPULELIQUID16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0HLACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
CALCIUM SULFIDEACTIVE INGREDIENT1MBW07J51QLACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07ILACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
MERCURIALIS PERENNISACTIVE INGREDIENTQ35465A1MALACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0HLACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
CALCIUM SULFIDEACTIVE MOIETY1MBW07J51QLACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07ILACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
MERCURIALIS PERENNISACTIVE MOIETYQ35465A1MALACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XLACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RLACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-6012LACHESIS BELLADONNA LIQUID [URIEL PHARMACY INC.]6Current NDC, Legacy NDC, 2 package rows20250109_c617a849-5043-43cd-974f-2f0d664fd468.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
Lachesis BelladonnaLACHESIS BELLADONNAUriel Pharmacy Inc.c617a849-5043-43cd-974f-2f0d664fd4682025-01-07WarningsExact identifier
ndc (product): 48951-6012

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-6012-14895160120110 AMPULE in 1 BOX (48951-6012-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent