Arnica Plus

Product NDC
57520-0630
11-digit product format
575200630
Labeler code
57520
Product ID
57520-0630_b20d5ffb-0b5a-493a-bc93-81f5018dfb1a
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica montana, Hamamelis virginiana, Rhus toxicodendron,
Dosage form
GEL
Route
TOPICAL
Labeler
Apotheca Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-10-20
Marketing end
2023-06-07
Substance
ARNICA MONTANA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; TOXICODENDRON PUBESCENS LEAF
Active strength
6 [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57520-0630-12022-04-28C16284748780-19d75b9d1-0ce1-f424-e053-dadaa90a57ce4fbda670-c27f-47d3-b661-72126cc67c84
57520-0630-12020-01-31C16284748780-19d75b9d1-0ce1-f424-e053-dadaa90a57ce4fbda670-c27f-47d3-b661-72126cc67c84

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57520-0630-157520063001105 g in 1 TUBE (57520-0630-1) 105 g2011-10-202023-06-07NoNoCurrent