FDA.reportPublic FDA data

ANTIMONIUM CRUDUM

Product NDC
60512-1003
11-digit product format
605121003
Labeler code
60512
Product ID
60512-1003_00d2c848-1dcb-469d-9d31-a5ac9ca1a201
Type
HUMAN OTC DRUG
Nonproprietary name
ANTIMONIUM CRUDUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ANTIMONY TRISULFIDE
Active strength
3 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1003-12025-12-31C16284748780-19d75b9d0-8785-f424-e053-dadaa90a57ce1eb7f477-0126-4f2b-b939-d8c8826ae5af
60512-1003-12020-01-31C16284748780-19d75b9d0-8785-f424-e053-dadaa90a57ce1eb7f477-0126-4f2b-b939-d8c8826ae5af

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANTIMONY TRISULFIDEACTIVE INGREDIENTF79059A38UANTIMONIUM CRUDUM PELLET [HOMEOLAB USA INC]1
ANTIMONY CATION (3+)ACTIVE MOIETY069647RPT5ANTIMONIUM CRUDUM PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANTIMONIUM CRUDUM PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554ANTIMONIUM CRUDUM PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1003ANTIMONIUM CRUDUM PELLET [HOMEOLAB USA INC]1Legacy NDC20111202_1eb7f477-0126-4f2b-b939-d8c8826ae5af.zip