Home NDC 75186-002-02 Primeauty
Product NDC 75186-002
Requested package NDC 75186-002-02
11-digit product format 751860002
Labeler code 75186
Product ID 75186-002_a3ec10bf-8e31-73da-e053-2a95a90a9107
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Huizhou Duomei Daily Necessities Co., Ltd.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-22
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 75 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…
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75186-002-01 PrimeautySqueeze Tube 10 mL in 1 TUBE LIQUID 10 1 75186-002-02 PrimeautySqueeze Tube 20 mL in 1 TUBE LIQUID 20 1 75186-002-03 PrimeautySqueeze Tube 30 mL in 1 TUBE LIQUID 30 1 75186-002-04 PrimeautySqueeze Tube 50 mL in 1 TUBE LIQUID 50 1 75186-002-05 PrimeautySqueeze Tube 60 mL in 1 TUBE LIQUID 60 1 75186-002-06 PrimeautySqueeze Tube 80 mL in 1 TUBE LIQUID 80 1 75186-002-07 PrimeautySqueeze Tube 100 mL in 1 TUBE LIQUID 100 1 75186-002-08 PrimeautySqueeze Tube 150 mL in 1 TUBE LIQUID 150 1 75186-002-09 PrimeautySqueeze Tube 200 mL in 1 TUBE LIQUID 200 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75186-002 PRIMEAUTY SQUEEZE TUBE (ETHYL ALCOHOL) LIQUID [HUIZHOU DUOMEI DAILY NECESSITIES CO., LTD.] 1 Legacy NDC, 9 package rows 20200423_a3ec0100-e6f2-e5df-e053-2995a90aaa23.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 75186-002-02 75186000202 20 mL in 1 TUBE (75186-002-02) 20 ml 2020-04-22 0000-00-00 No No Current