Arnica e pl. tota 6

Product NDC
48951-1132
11-digit product format
489511132
Labeler code
48951
Product ID
48951-1132_4bd3d3b4-ffd0-a5e4-e063-6394a90af732
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica e pl. tota 6
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ARNICA MONTANA
Active strength
6 [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
Arnica e pl. tota 6
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA6 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1132-1Arnica e pl. tota 61 mL in 1 AMPULELIQUID15
48951-1132-1Arnica e pl. tota 610 in 1 BOXLIQUID105

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1132ARNICA E PL. TOTA 6 LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20241123_d84176b5-8e86-4055-abf5-f4a80ad4334f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1132-14895111320110 AMPULE in 1 BOX (48951-1132-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent