Cereus

Product NDC
49693-2001
11-digit product format
496932001
Labeler code
49693
Product ID
49693-2001_323bf388-43f1-42de-adc8-265ca164aa6f
Type
HUMAN OTC DRUG
Nonproprietary name
Bacillus cereus
Dosage form
LIQUID
Route
ORAL
Labeler
USPharmaCo
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-12-15
Marketing end
0000-00-00
Substance
BACILLUS CEREUS
Active strength
6 [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
49693-2001-12019-10-21C16284748780-1956f9ecf-d296-621f-e053-dbdaa90a74adCEREUS DROPS 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49693-2001-1Cereus5 mL in 1 BOTTLELIQUID51
49693-2001-1Cereus1 in 1 BOXLIQUID11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Bacillus cereusACTIVE INGREDIENT7YC151N82LCEREUS (BACILLUS CEREUS) LIQUID [USPHARMACO]1
Bacillus cereusACTIVE MOIETY7YC151N82LCEREUS (BACILLUS CEREUS) LIQUID [USPHARMACO]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49693-2001CEREUS (BACILLUS CEREUS) LIQUID [USPHARMACO]1Legacy NDC, 2 package rows20091223_103ff21b-8c53-4c73-86fe-78ea644f1303.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
49693-2001-1496932001015 mL in 1 BOTTLE5 mlHistorical