FDA.reportPublic FDA data

Aurum Equisetum B

Product NDC
48951-1188
Requested package NDC
48951-1188-1
11-digit product format
489511188
Labeler code
48951
Product ID
48951-1188_6c689177-addd-55f3-e053-2991aa0a171d
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum Equisetum B
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
EQUISETUM ARVENSE TOP; GOLD
Active strength
17 [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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-118848951-1188-1IInactivated 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
48951-1188-1Aurum Equisetum B1 mL in 1 AMPULELIQUID13
48951-1188-1Aurum Equisetum B10 in 1 BOXLIQUID103

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZAURUM EQUISETUM B LIQUID [URIEL PHARMACY INC.]1
GOLDACTIVE INGREDIENT79Y1949PYOAURUM EQUISETUM B LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZAURUM EQUISETUM B LIQUID [URIEL PHARMACY INC.]1
GOLDACTIVE MOIETY79Y1949PYOAURUM EQUISETUM B LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAURUM EQUISETUM B LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAURUM EQUISETUM B LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1188AURUM EQUISETUM B LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20180517_5cdb62a8-a27f-40b4-bc3a-0e45ae4b57e6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1188-14895111880110 AMPULE in 1 BOX (48951-1188-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent