Home NDC 0132-8743-02 SUMMERS EVE
Product NDC 0132-8743
Requested package NDC 0132-8743-02
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2020-06-10 20:45 UTC · source 2020-06-10 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POVIDONE-IODINE ACTIVE INGREDIENT 85H0HZU99M SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8 IODINE ACTIVE MOIETY 9679TC07X4 SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8 ANHYDROUS CITRIC ACID INACTIVE INGREDIENT XF417D3PSL SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8 SODIUM PHOSPHATE, TRIBASIC ANHYDROUS INACTIVE INGREDIENT SX01TZO3QZ SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8 WATER INACTIVE INGREDIENT 059QF0KO0R SUMMERS EVE (POVIDONE-IODINE) DOUCHE [C.B. FLEET COMPANY, INC.] 8
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0132-8743-02 00132874302 133 mL in 1 BOTTLE (0132-8743-02) 133 ml 2002-05-10 0000-00-00 No No Current