Equisetum Formica

Product NDC
48951-4035
11-digit product format
489514035
Labeler code
48951
Product ID
48951-4035_4bd40b65-06f9-de90-e063-6394a90afafb
Type
HUMAN OTC DRUG
Nonproprietary name
Equisetum Formica
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
EQUISETUM ARVENSE TOP; FORMICA RUFA
Active strength
17; 6 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Equisetum Formica
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FORMICA RUFA17 [hp_X]/mL
EQUISETUM ARVENSE TOP6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
55H0W83JO5Internal UNII lookup
1DP6Y6B65ZInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a88afb03-3ddd-4117-ac3d-28a1beb32b6cAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4035-1Equisetum Formica10 in 1 BOXLIQUID104
48951-4035-1Equisetum Formica1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZEQUISETUM FORMICA LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE INGREDIENT55H0W83JO5EQUISETUM FORMICA LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZEQUISETUM FORMICA LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE MOIETY55H0W83JO5EQUISETUM FORMICA LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XEQUISETUM FORMICA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0REQUISETUM FORMICA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4035EQUISETUM FORMICA LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 2 package rows20180425_a88afb03-3ddd-4117-ac3d-28a1beb32b6c.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
Equisetum FormicaEQUISETUM FORMICAUriel Pharmacy Inc.a88afb03-3ddd-4117-ac3d-28a1beb32b6c2026-02-27WarningsExact identifier
ndc (product): 48951-4035

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4035-14895140350110 AMPULE in 1 BOX (48951-4035-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent