Arnica e rad. 12

Product NDC
48951-1135
11-digit product format
489511135
Labeler code
48951
Product ID
48951-1135_6d80e52a-ad92-b8f2-e053-2a91aa0ac605
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica e rad. 12
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ARNICA MONTANA ROOT
Active strength
12 [hp_X]/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1135-2Arnica e rad. 121350 in 1 BOTTLE, GLASSPELLET13502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1135ARNICA E RAD. 12 PELLET [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20180531_e90a7cf5-6585-462c-b69c-bda0b83ab0a7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1135-2489511135021350 PELLET in 1 BOTTLE, GLASS (48951-1135-2) 1350 pellet2009-09-010000-00-00NoNoCurrent