Home NDC 80371-103-01 Biolustre Liquid Disinfectant
Product NDC 80371-103
Requested package NDC 80371-103-01
11-digit product format 803710103
Labeler code 80371
Product ID 80371-103_ae3815c5-f9ba-7f2d-e053-2995a90a5bc3
Type HUMAN OTC DRUG
Nonproprietary name Alcochol
Dosage form LIQUID
Route TOPICAL
Labeler KOYUNCU BILISIM TEKNOLOJILERI SANAYI VE TICARET LIMITED SIRKETI
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-08-31
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 · 15 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…
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 80371-103-01 Biolustre Liquid Disinfectant 50 mL in 1 BOTTLE, PLASTIC LIQUID 50 1 80371-103-02 Biolustre Liquid Disinfectant 100 mL in 1 BOTTLE, PLASTIC LIQUID 100 1 80371-103-03 Biolustre Liquid Disinfectant 250 mL in 1 BOTTLE, PLASTIC LIQUID 250 1 80371-103-04 Biolustre Liquid Disinfectant 500 mL in 1 BOTTLE, PLASTIC LIQUID 500 1 80371-103-05 Biolustre Liquid Disinfectant 1000 mL in 1 BOTTLE, PUMP LIQUID 1000 1 80371-103-06 Biolustre Liquid Disinfectant 5000 mL in 1 BOTTLE, PLASTIC LIQUID 5000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80371-103 BIOLUSTRE LIQUID DISINFECTANT (ALCOCHOL) LIQUID [KOYUNCU BILISIM TEKNOLOJILERI SANAYI VE TICARET LIMITED SIRKETI] 1 Legacy NDC, 6 package rows 20200901_ae3815c5-f9b9-7f2d-e053-2995a90a5bc3.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 80371-103-01 80371010301 50 mL in 1 BOTTLE, PLASTIC (80371-103-01) 50 ml 2020-08-31 0000-00-00 No No Current