Home NDC 79129-003-02 B-GOOD HAND AND SKIN DISINFECTING AGENT
Product NDC 79129-003
Requested package NDC 79129-003-02
11-digit product format 791290003
Labeler code 79129
Product ID 79129-003_a98ea8b6-b694-1e9c-e053-2a95a90a5e4e
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form SOLUTION
Route TOPICAL
Labeler HONNES SAGLIK VE ENDUSTRIYEL URUNLERI ANONIM SIRKETI
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-03-30
Marketing end 0000-00-00
Substance CHLORHEXIDINE GLUCONATE; ALCOHOL
Active strength 4 mg/100mL; 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79129-003-01 B-GOOD HAND AND SKIN DISINFECTING AGENT 100 mL in 1 BOTTLE, PLASTIC SOLUTION 100 1 79129-003-02 B-GOOD HAND AND SKIN DISINFECTING AGENT 1000 mL in 1 BOTTLE, PLASTIC SOLUTION 1000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79129-003 B-GOOD HAND AND SKIN DISINFECTING AGENT (ALCOHOL) SOLUTION [HONNES SAGLIK VE ENDUSTRIYEL URUNLERI ANONIM SIRKETI] 1 Legacy NDC, 2 package rows 20200709_a98ea8b6-b6a2-1e9c-e053-2a95a90a5e4e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 79129-003-02 79129000302 1000 mL in 1 BOTTLE, PLASTIC (79129-003-02) 1000 ml 2020-03-30 0000-00-00 No No Current