Astragalus Arnica

Product NDC
48951-1171
Type
HUMAN OTC DRUG
Nonproprietary name
Astragalus Arnica
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
ARNICA MONTANA; ASTRAGALUS PROPINQUUS ROOT
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
48951-1171-360 mL in 1 BOTTLE, GLASS (48951-1171-3) 2009-09-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Astragalus ArnicaUriel Pharmacy Inc.2026-02-27HUMAN OTC DRUG LABEL5