Advanced Arnica

Product NDC
57955-7304
11-digit product format
579557304
Labeler code
57955
Product ID
57955-7304_454592ca-4a4d-47cd-8387-7ab93d98955c
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica montana, Arnica montana, radix
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-05-31
Marketing end
0000-00-00
Substance
ARNICA MONTANA; ARNICA MONTANA ROOT
Active strength
6 [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-7304-22020-01-31C16284748780-19d75b9d0-5212-f424-e053-dadaa90a57ceAdvanced Arnica

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-7304-2Advanced Arnica59 mL in 1 BOTTLE, SPRAYLIQUID592

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-7304ADVANCED ARNICA (ARNICA MONTANA, ARNICA MONTANA, RADIX) LIQUID [KING BIO INC.]2Legacy NDC, 1 package rows20180601_48c0b84f-13f0-4f63-bff8-7e600be51059.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
57955-7304-25795573040259 mL in 1 BOTTLE, SPRAY59 mlHistorical