Home NDC 73764-002-05 Ethyl Alcohol
Product NDC 73764-002
Requested package NDC 73764-002-05
11-digit product format 737640002
Labeler code 73764
Product ID 73764-002_a736596e-6da4-37a1-e053-2995a90ac312
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler Marine Essence Biosciences Corporation of USA
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-03-23
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 80 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 · 19 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…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73764-002-01 Ethyl Alcohol 500 mL in 1 BOTTLE, PUMP GEL 500 3 73764-002-02 Ethyl Alcohol 236 mL in 1 BOTTLE, PUMP GEL 236 3 73764-002-03 Ethyl Alcohol 177 mL in 1 BOTTLE, PUMP GEL 177 3 73764-002-04 Ethyl Alcohol 473 mL in 1 BOTTLE, PUMP GEL 473 3 73764-002-05 Ethyl Alcohol 250 mL in 1 BOTTLE, PUMP GEL 250 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73764-002 ETHYL ALCOHOL GEL [MARINE ESSENCE BIOSCIENCES CORPORATION OF USA] 3 Legacy NDC, 5 package rows 20200605_a1ba4cc4-969e-1c96-e053-2995a90ad2ff.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 73764-002-05 73764000205 250 mL in 1 BOTTLE, PUMP (73764-002-05) 250 ml 2020-06-01 0000-00-00 No No Current