Home NDC 75186-001-05 Primeauty
Product NDC 75186-001
Requested package NDC 75186-001-05
11-digit product format 751860001
Labeler code 75186
Product ID 75186-001_a3ebb123-c493-13fe-e053-2a95a90a0842
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 2020-04-22
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…
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 75186-001-01 PrimeautyBottle (Pump) 240 mL in 1 BOTTLE, PUMP LIQUID 240 1 75186-001-02 PrimeautyBottle (Pump) 250 mL in 1 BOTTLE, PUMP LIQUID 250 1 75186-001-03 PrimeautyBottle (Pump) 300 mL in 1 BOTTLE, PUMP LIQUID 300 1 75186-001-04 PrimeautyBottle (Pump) 350 mL in 1 BOTTLE, PUMP LIQUID 350 1 75186-001-05 PrimeautyBottle (Pump) 400 mL in 1 BOTTLE, PUMP LIQUID 400 1 75186-001-06 PrimeautyBottle (Pump) 500 mL in 1 BOTTLE, PUMP LIQUID 500 1 75186-001-07 PrimeautyBottle (Pump) 1000 mL in 1 BOTTLE, PUMP LIQUID 1000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75186-001 PRIMEAUTY BOTTLE (PUMP) (ALCOHOL) LIQUID [HUIZHOU DUOMEI DAILY NECESSITIES CO., LTD.] 1 Legacy NDC, 7 package rows 20200423_a3ebb112-80b3-6a54-e053-2995a90a730c.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 75186-001-05 75186000105 400 mL in 1 BOTTLE, PUMP (75186-001-05) 400 ml 2020-04-22 0000-00-00 No No Current