FDA.reportPublic FDA data

Arnica Aurum 20/30

Product NDC
48951-1106
11-digit product format
489511106
Labeler code
48951
Product ID
48951-1106_44840be2-b7bb-ba38-e063-6394a90a0e38
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Aurum 20/30
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ARNICA MONTANA; GOLD; HYOSCYAMUS NIGER LEAF; ONOPORDUM ACANTHIUM FLOWER; PRIMULA VERIS FLOWER
Active strength
20; 30; 4; 3; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arnica Aurum 20/30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA20 [hp_X]/mL
GOLD30 [hp_X]/mL
HYOSCYAMUS NIGER LEAF4 [hp_X]/mL
ONOPORDUM ACANTHIUM FLOWER3 [hp_X]/mL
PRIMULA VERIS FLOWER3 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW, 79Y1949PYO, 32IT7G8BAW, AP97AUF88E, W5BET37294

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1106-1Arnica Aurum 20/301 mL in 1 AMPULELIQUID15
48951-1106-1Arnica Aurum 20/3010 in 1 BOXLIQUID105

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1106ARNICA AURUM 20/30 LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20240120_9ebdcfa6-f8b1-4a25-9008-e9f923ec9ffd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1106-14895111060110 AMPULE in 1 BOX (48951-1106-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent