Arnica Forte

Product NDC
48951-1308
11-digit product format
489511308
Labeler code
48951
Product ID
48951-1308_77f72303-08a7-a101-e053-2991aa0a62eb
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Forte
Dosage form
GEL
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ARNICA MONTANA FLOWER
Active strength
1 [hp_X]/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-1308-52026-01-29C16284748780-149896155-aa4d-586f-e063-e6dba90add90Arnica Forte

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1308-5Arnica Forte60 g in 1 TUBEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1308ARNICA FORTE GEL [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20181012_77f72303-08a6-a101-e053-2991aa0a62eb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1308-54895113080560 g in 1 TUBE (48951-1308-5) 60 g2009-09-010000-00-00NoNoCurrent