Mucor

Product NDC
49693-1301
11-digit product format
496931301
Labeler code
49693
Product ID
49693-1301_87f66e2e-ffef-400b-bf7a-cfff9d99e14a
Type
HUMAN OTC DRUG
Nonproprietary name
Mucor racemosus
Dosage form
LIQUID
Route
ORAL
Labeler
USPharmaCo
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-12-15
Marketing end
0000-00-00
Substance
MUCOR RACEMOSUS
Active strength
4 [hp_X]/10mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49693-1301-12019-10-21C16284748780-1956f9ecf-cc24-621f-e053-dbdaa90a74adMUCOR DROPS 4X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49693-1301-1Mucor10 mL in 1 BOTTLELIQUID101
49693-1301-1Mucor1 in 1 BOXLIQUID11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Mucor racemosusACTIVE INGREDIENT17RH99LQ7GMUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO]1
Mucor racemosusACTIVE MOIETY17RH99LQ7GMUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49693-1301MUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO]1Legacy NDC, 2 package rows20091228_e9f31592-ec62-48b6-b12b-503b8ad81d78.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
49693-1301-14969313010110 mL in 1 BOTTLE10 mlHistorical