Home NDC 51774-004-12 PURIDERM
Product NDC 51774-004
Requested package NDC 51774-004-12
11-digit product format 517740004
Labeler code 51774
Product ID 51774-004_c43c4ef1-5ed8-4746-9c26-e6826014bdb1
Type HUMAN OTC DRUG
Nonproprietary name benzalkonium chloride
Dosage form LIQUID
Route TOPICAL
Labeler INDUSTRIAS CHAMER S.A. DE C.V.
Application part333E
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-08-24
Marketing end 0000-00-00
Substance BENZALKONIUM CHLORIDE
Active strength 1 mg/mL
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 51774-004-08 PURIDERM ANTIBACTERIAL 240 mL in 1 BOTTLE LIQUID 240 1 51774-004-12 PURIDERM ANTIBACTERIAL 360 mL in 1 BOTTLE LIQUID 360 1 51774-004-16 PURIDERM ANTIBACTERIAL 480 mL in 1 BOTTLE LIQUID 480 1 51774-004-28 PURIDERM ANTIBACTERIAL 3785 mL in 1 BOTTLE LIQUID 3785 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51774-004 PURIDERM ANTIBACTERIAL (BENZALKONIUM CHLORIDE) LIQUID [INDUSTRIAS CHAMER S.A. DE C.V.] 1 Legacy NDC, 4 package rows 20200824_39a58164-a4ea-4876-9ef5-dc45be4ecf79.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 51774-004-12 51774000412 360 mL in 1 BOTTLE (51774-004-12) 360 ml 2020-08-24 0000-00-00 No No Current