Home NDC 12745-180-01 AloeSafe
Product NDC 12745-180
Requested package NDC 12745-180-01
11-digit product format 127450180
Labeler code 12745
Product ID 12745-180_55921e21-efe4-da39-e063-6294a90a6d27
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 2010-07-01
Substance ALCOHOL
Active strength 60 g/100mL
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 AloeSafe
Brand name suffix Antiseptic Hand Sanitizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 60 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M 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 12745-180-01 AloeSafeAntiseptic Hand Sanitizer 60 mL in 1 BOTTLE, PLASTIC LIQUID 60 4 12745-180-02 AloeSafeAntiseptic Hand Sanitizer 120 mL in 1 BOTTLE, PLASTIC LIQUID 120 4 12745-180-03 AloeSafeAntiseptic Hand Sanitizer 480 mL in 1 BOTTLE, PLASTIC LIQUID 480 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 12745-180 ALOESAFE ANTISEPTIC HAND SANITIZER (ETHYL ALCOHOL) LIQUID [MEDICAL CHEMICAL CORPORATION] 3 Current NDC, Legacy NDC, 3 package rows 20220118_950f012e-7908-523c-e053-2995a90afa6b.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 12745-180-01 12745018001 60 mL in 1 BOTTLE, PLASTIC (12745-180-01) 60 ml 2019-10-14 0000-00-00 No No Current