Home NDC 76802-100-04 MediPlus
Product NDC 76802-100
Requested package NDC 76802-100-04
11-digit product format 768020100
Labeler code 76802
Product ID 76802-100_3e0f1b13-e98d-41cb-b2bd-7ee6c8cf99aa
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler LIX DETERGENT JOINT STOCK COMPANY
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-29
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 70 mL/100mL
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 · 18 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…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…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76802-100-01 MediPlus 100 mL in 1 BOTTLE LIQUID 100 1 76802-100-02 MediPlus 250 mL in 1 BOTTLE LIQUID 250 1 76802-100-03 MediPlus 500 mL in 1 BOTTLE LIQUID 500 1 76802-100-04 MediPlus 1000 mL in 1 BOTTLE LIQUID 1000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76802-100 MEDIPLUS (ETHYL ALCOHOL) LIQUID [LIX DETERGENT JOINT STOCK COMPANY] 1 Legacy NDC, 4 package rows 20200508_c3149f92-d8f7-4160-bc42-2acd910aeba2.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76802-100-04 76802010004 1000 mL in 1 BOTTLE (76802-100-04) 1000 ml 2020-04-29 0000-00-00 No No Current