Home NDC 75186-000-10 Primeauty
Product NDC 75186-000
Requested package NDC 75186-000-10
11-digit product format 751860000
Labeler code 75186
Product ID 75186-000_a38226a7-2ee3-569b-e053-2a95a90a22d3
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form LIQUID
Route TOPICAL
Labeler Huizhou Duomei Daily Necessities Co., Ltd.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-17
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…
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 75186-000-03 PrimeautyBottle (Screw Cap) 30 mL in 1 BOTTLE LIQUID 30 1 75186-000-04 PrimeautyBottle (Screw Cap) 50 mL in 1 BOTTLE LIQUID 50 1 75186-000-05 PrimeautyBottle (Screw Cap) 60 mL in 1 BOTTLE LIQUID 60 1 75186-000-06 PrimeautyBottle (Screw Cap) 100 mL in 1 BOTTLE LIQUID 100 1 75186-000-07 PrimeautyBottle (Screw Cap) 150 mL in 1 BOTTLE LIQUID 150 1 75186-000-08 PrimeautyBottle (Screw Cap) 200 mL in 1 BOTTLE LIQUID 200 1 75186-000-09 PrimeautyBottle (Screw Cap) 80 mL in 1 BOTTLE LIQUID 80 1 75186-000-10 PrimeautyBottle (Screw Cap) 250 mL in 1 BOTTLE LIQUID 250 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75186-000 PRIMEAUTY BOTTLE (SCREW CAP) (ALCOHOL) LIQUID [HUIZHOU DUOMEI DAILY NECESSITIES CO., LTD.] 1 Legacy NDC, 8 package rows 20200423_a382270c-0505-d2eb-e053-2995a90a6ec0.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 75186-000-10 75186000010 250 mL in 1 BOTTLE (75186-000-10) 250 ml 2020-04-17 0000-00-00 No No Current