Home NDC 12745-177-01 Medi Fect
Product NDC 12745-177
Requested package NDC 12745-177-01
11-digit product format 127450177
Labeler code 12745
Product ID 12745-177_559190f3-0f95-df54-e063-6294a90a8199
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Medical Chemical Corporation
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2001-05-14
Substance ALCOHOL; DIAZOLIDINYL UREA
Active strength 59.86; 1 g/100mL; g/100mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 13 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Medi Fect
Brand name suffix Antiseptic Hand Wash
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 59.86 g/100mL DIAZOLIDINYL UREA 1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup H5RIZ3MPW4 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 12745-177-01 Medi FectAntiseptic Hand Wash 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 16 12745-177-02 Medi FectAntiseptic Hand Wash 473 mL in 1 BOTTLE, PLASTIC LIQUID 473 16 12745-177-03 Medi FectAntiseptic Hand Wash 3785 mL in 1 BOTTLE, PLASTIC LIQUID 3785 16 12745-177-04 Medi FectAntiseptic Hand Wash 18927 mL in 1 BOTTLE, PLASTIC LIQUID 18927 16 12745-177-05 Medi FectAntiseptic Hand Wash 59 mL in 1 BOTTLE, PLASTIC LIQUID 59 16 12745-177-06 Medi FectAntiseptic Hand Wash 237 mL in 1 BOTTLE, PLASTIC LIQUID 237 16 12745-177-07 Medi FectAntiseptic Hand Wash 946 mL in 1 BOTTLE, PLASTIC LIQUID 946 16 12745-177-08 Medi FectAntiseptic Hand Wash 208198 mL in 1 DRUM LIQUID 208198 16
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 12745-177 MEDI FECT ANTISEPTIC HAND WASH (ETHYL ALCOHOL) LIQUID [MEDICAL CHEMICAL CORPORATION] 15 Current NDC, Legacy NDC, 8 package rows 20220118_dc397d9c-9c12-41e5-ab7f-196fcad5bf97.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 9 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 12745-177-01 12745017701 118 mL in 1 BOTTLE, PLASTIC (12745-177-01) 118 ml 2001-05-14 0000-00-00 No No Current