FDA.reportPublic FDA data

BENZOICUM ACIDUM

Product NDC
60512-6203
11-digit product format
605126203
Labeler code
60512
Product ID
60512-6203_1425368a-1c7d-4dbc-bd0b-34d1d25fb20a
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOICUM ACIDUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
BENZOIC ACID
Active strength
2 [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
60512-6203-12025-12-30C16284748780-19d75b9cf-da21-f424-e053-dadaa90a57ce32eca548-09b1-40b1-acc7-372ec50fadfe
60512-6203-12020-01-31C16284748780-19d75b9cf-da21-f424-e053-dadaa90a57ce32eca548-09b1-40b1-acc7-372ec50fadfe

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BENZOIC ACIDACTIVE INGREDIENT8SKN0B0MIMBENZOICUM ACIDUM PELLET [HOMEOLAB USA INC.]1
BENZOIC ACIDACTIVE MOIETY8SKN0B0MIMBENZOICUM ACIDUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GBENZOICUM ACIDUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554BENZOICUM ACIDUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6203BENZOICUM ACIDUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_32eca548-09b1-40b1-acc7-372ec50fadfe.zip