FDA.reportPublic FDA data

ABIES CANADENSIS

Product NDC
60512-6436
11-digit product format
605126436
Labeler code
60512
Product ID
60512-6436_26314bf2-eb27-4cf6-ae2c-8f88d8bfd670
Type
HUMAN OTC DRUG
Nonproprietary name
ABIES CANADENSIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
TSUGA CANADENSIS BARK
Active strength
1 [hp_X]/1
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
60512-6436-12025-12-31C16284748780-19d75b9cf-d49f-f424-e053-dadaa90a57ce90581b0e-243b-403b-ab38-081299341f37
60512-6436-12020-01-31C16284748780-19d75b9cf-d49f-f424-e053-dadaa90a57ce90581b0e-243b-403b-ab38-081299341f37

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TSUGA CANADENSIS BARKACTIVE INGREDIENTR53V5F950SABIES CANADENSIS PELLET [HOMEOLAB USA INC.]1
TSUGA CANADENSIS BARKACTIVE MOIETYR53V5F950SABIES CANADENSIS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GABIES CANADENSIS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ABIES CANADENSIS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6436ABIES CANADENSIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_90581b0e-243b-403b-ab38-081299341f37.zip