FDA.reportPublic FDA data

Sambucus Larix

Product NDC
48951-8162
11-digit product format
489518162
Labeler code
48951
Product ID
48951-8162_6cf487e7-7d05-27c9-e053-2991aa0af305
Type
HUMAN OTC DRUG
Nonproprietary name
Sambucus Larix
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
BLACK COHOSH; SAMBUCUS NIGRA FLOWERING TOP; LARIX DECIDUA RESIN
Active strength
3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-8162IInactivated by FDA2026-10-15
excluded packagepackage48951-816248951-8162-1IInactivated by FDA2026-10-15

Reported adverse events (FAERS/openFDA)#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8162-1Sambucus Larix1 mL in 1 AMPULELIQUID12
48951-8162-1Sambucus Larix10 in 1 BOXLIQUID102

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BLACK COHOSHACTIVE INGREDIENTK73E24S6X9SAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1
LARIX DECIDUA RESINACTIVE INGREDIENTAD8LJ73GQFSAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1
SAMBUCUS NIGRA FLOWERING TOPACTIVE INGREDIENTCT03BSA18USAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1
BLACK COHOSHACTIVE MOIETYK73E24S6X9SAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1
LARIX DECIDUA RESINACTIVE MOIETYAD8LJ73GQFSAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1
SAMBUCUS NIGRA FLOWERING TOPACTIVE MOIETYCT03BSA18USAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XSAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RSAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8162SAMBUCUS LARIX LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20180524_ce51d1cc-3714-4813-9df7-d990fc192401.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8162-14895181620110 AMPULE in 1 BOX (48951-8162-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent