Astragalus Formica

Product NDC
48951-1174
11-digit product format
489511174
Labeler code
48951
Product ID
48951-1174_4bae0a05-ae26-cd5d-e063-6394a90ab841
Type
HUMAN OTC DRUG
Nonproprietary name
Astragalus Formica
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ARNICA MONTANA; ASTRAGALUS PROPINQUUS ROOT; FORMICA RUFA; SILVER
Active strength
3; 3; 6; 30 [hp_X]/mL; [hp_X]/mL; [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
Astragalus Formica
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA3 [hp_X]/mL
ASTRAGALUS PROPINQUUS ROOT3 [hp_X]/mL
FORMICA RUFA6 [hp_X]/mL
SILVER30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O80TY208ZWInternal UNII lookup
922OP8YUPFInternal UNII lookup
55H0W83JO5Internal UNII lookup
3M4G523W1GInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
63230d4e-9c45-4d1e-83c9-80df269a6c3dAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1174-1Astragalus Formica1 mL in 1 AMPULELIQUID17
48951-1174-1Astragalus Formica10 in 1 BOXLIQUID107

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
ASTRAGALUS PROPINQUUS ROOTACTIVE INGREDIENT922OP8YUPFASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE INGREDIENT55H0W83JO5ASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE INGREDIENT3M4G523W1GASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
ARNICA MONTANAACTIVE MOIETYO80TY208ZWASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
ASTRAGALUS PROPINQUUS ROOTACTIVE MOIETY922OP8YUPFASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE MOIETY55H0W83JO5ASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE MOIETY3M4G523W1GASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1174ASTRAGALUS FORMICA LIQUID [URIEL PHARMACY INC.]6Current NDC, Legacy NDC, 2 package rows20241127_63230d4e-9c45-4d1e-83c9-80df269a6c3d.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
Astragalus FormicaASTRAGALUS FORMICAUriel Pharmacy Inc.63230d4e-9c45-4d1e-83c9-80df269a6c3d2026-02-25WarningsExact identifier
ndc (product): 48951-1174

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1174-14895111740110 AMPULE in 1 BOX (48951-1174-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent