Mucor

Product NDC
49693-1306
11-digit product format
496931306
Labeler code
49693
Product ID
49693-1306_bb64565a-3f29-4b46-be43-84373e03c67f
Type
HUMAN OTC DRUG
Nonproprietary name
Mucor racemosus
Dosage form
LIQUID
Route
OPHTHALMIC
Labeler
USPharmaCo
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-12-15
Marketing end
0000-00-00
Substance
MUCOR RACEMOSUS
Active strength
5 [hp_X]/5mL
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
49693-1306-12019-10-21C16284748780-1956f9ecf-dc9e-621f-e053-dbdaa90a74adMUCOR EYE DROPS 5X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49693-1306-1Mucor5 mL in 1 BOTTLELIQUID52
49693-1306-1Mucor1 in 1 BOXLIQUID12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Mucor racemosusACTIVE INGREDIENT17RH99LQ7GMUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO]2
Mucor racemosusACTIVE MOIETY17RH99LQ7GMUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49693-1306MUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO]2Legacy NDC, 2 package rows20100116_9023368b-eecd-458f-b332-84d0495dc94a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
49693-1306-1496931306015 mL in 1 BOTTLE5 mlHistorical