Arnica comp.

Product NDC
48951-1339
Requested package NDC
48951-1339-1
11-digit product format
489511339
Labeler code
48951
Product ID
48951-1339_b6acddc9-b4f4-4b25-e053-2995a90a175e
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica comp.
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ECHINACEA, UNSPECIFIED; BAPTISIA AUSTRALIS ROOT; SOLANUM DULCAMARA FLOWER; SOLANUM NIGRUM FRUIT; MERCURIALIS PERENNIS; ARNICA MONTANA; SOLANUM LYCOPERSICUM FRUITING TOP; APIS MELLIFERA; EUCALYPTUS GUM; COLCHICUM AUTUMNALE WHOLE; BRYONIA ALBA ROOT; EUPATORIUM CANNABINUM FLOWERING TOP; BENZOIC ACID; TOXICODENDRON PUBESCENS LEAF
Active strength
4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-133948951-1339-1IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1339-1Arnica comp.1 mL in 1 AMPULELIQUID11
48951-1339-1Arnica comp.10 in 1 BOXLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1339ARNICA COMP. LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20201218_b6acddc9-b4f3-4b25-e053-2995a90a175e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1339-14895113390110 AMPULE in 1 BOX (48951-1339-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent