SUMMERS EVE

Product NDC
0132-8743
11-digit product format
001328743
Labeler code
0132
Product ID
0132-8743_26c73f2b-f79c-43a5-b4b7-6300debaf90f
Type
HUMAN OTC DRUG
Nonproprietary name
povidone-iodine
Dosage form
DOUCHE
Route
VAGINAL
Labeler
C.B. Fleet Company, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2002-05-10
Marketing end
0000-00-00
Substance
POVIDONE-IODINE
Active strength
4 g/133mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0132-8743-022020-06-30C16284748780-19d75b9d0-1336-f424-e053-dadaa90a57ce46f59721-0d24-4b42-ab3b-b250744da1e3
0132-8743-022020-01-31C16284748780-19d75b9d0-1336-f424-e053-dadaa90a57ce46f59721-0d24-4b42-ab3b-b250744da1e3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0132-8743-02ML - Milliliter0132-8743922c2231-0832-4c38-9d81-26f68f1ef43212013-09-04

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0132-8743-0200132874302133 mL in 1 BOTTLE (0132-8743-02) 133 ml2002-05-100000-00-00NoNoCurrent