Solum Aesculus

Product NDC
48951-8193
11-digit product format
489518193
Labeler code
48951
Product ID
48951-8193_448429f6-d4a6-e023-e063-6394a90adbf1
Type
HUMAN OTC DRUG
Nonproprietary name
Solum Aesculus
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
EQUISETUM ARVENSE TOP; HORSE CHESTNUT; SPHAGNUM SQUARROSUM PEAT; ST. JOHN'S WORT
Active strength
3; 3; 3; 3 [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
Solum Aesculus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HORSE CHESTNUT3 [hp_X]/mL
EQUISETUM ARVENSE TOP3 [hp_X]/mL
ST. JOHN'S WORT3 [hp_X]/mL
SPHAGNUM SQUARROSUM PEAT3 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3C18L6RJAZInternal UNII lookup
1DP6Y6B65ZInternal UNII lookup
UFH8805FKAInternal UNII lookup
Z7G226H5SAInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
e3f39461-e27d-419a-8271-eb96457be189Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8193-1Solum Aesculus1 mL in 1 AMPULELIQUID18
48951-8193-1Solum Aesculus10 in 1 BOXLIQUID108

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZSOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
HORSE CHESTNUTACTIVE INGREDIENT3C18L6RJAZSOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
SPHAGNUM SQUARROSUM PEATACTIVE INGREDIENTZ7G226H5SASOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
ST. JOHN'S WORTACTIVE INGREDIENTUFH8805FKASOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZSOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
HORSE CHESTNUTACTIVE MOIETY3C18L6RJAZSOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
SPHAGNUM SQUARROSUM PEATACTIVE MOIETYZ7G226H5SASOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
ST. JOHN'S WORTACTIVE MOIETYUFH8805FKASOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XSOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RSOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8193SOLUM AESCULUS LIQUID [URIEL PHARMACY INC.]7Current NDC, Legacy NDC, 2 package rows20250109_e3f39461-e27d-419a-8271-eb96457be189.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
Solum AesculusSOLUM AESCULUSUriel Pharmacy Inc.e3f39461-e27d-419a-8271-eb96457be1892025-11-26WarningsExact identifier
ndc (product): 48951-8193

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8193-14895181930110 AMPULE in 1 BOX (48951-8193-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent