Astragalus Arnica

Product NDC
48951-1171
11-digit product format
489511171
Labeler code
48951
Product ID
48951-1171_4bd3fa49-f046-6e91-e063-6294a90abe66
Type
HUMAN OTC DRUG
Nonproprietary name
Astragalus Arnica
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ASTRAGALUS PROPINQUUS ROOT; ARNICA MONTANA
Active strength
3; 30 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Astragalus Arnica
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ASTRAGALUS PROPINQUUS ROOT3 [hp_X]/mL
ARNICA MONTANA30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
922OP8YUPFInternal UNII lookup
O80TY208ZWInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f6296548-4d16-4690-a1a5-76d8bd718afaAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1171-3Astragalus Arnica60 mL in 1 BOTTLE, GLASSLIQUID605

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWASTRAGALUS ARNICA LIQUID [URIEL PHARMACY INC.]1
ASTRAGALUS PROPINQUUS ROOTACTIVE INGREDIENT922OP8YUPFASTRAGALUS ARNICA LIQUID [URIEL PHARMACY INC.]1
ARNICA MONTANAACTIVE MOIETYO80TY208ZWASTRAGALUS ARNICA LIQUID [URIEL PHARMACY INC.]1
ASTRAGALUS PROPINQUUS ROOTACTIVE MOIETY922OP8YUPFASTRAGALUS ARNICA LIQUID [URIEL PHARMACY INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MASTRAGALUS ARNICA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RASTRAGALUS ARNICA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1171ASTRAGALUS ARNICA LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 1 package rows20180417_f6296548-4d16-4690-a1a5-76d8bd718afa.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 ArnicaASTRAGALUS ARNICAUriel Pharmacy Inc.f6296548-4d16-4690-a1a5-76d8bd718afa2026-02-27WarningsExact identifier
ndc (product): 48951-1171

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1171-34895111710360 mL in 1 BOTTLE, GLASS (48951-1171-3) 60 ml2009-09-010000-00-00NoNoCurrent