Home NDC 81314-201-03 WANCARE
Product NDC 81314-201
Requested package NDC 81314-201-03
11-digit product format 813140201
Labeler code 81314
Product ID 81314-201_4fb64a2e-0dc9-4a06-a918-9aedcc8e8f43
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler KAF GRUP SAGLIK HIZMETLERI INSAAT SANAYI VE TICARET LIMITED SIRKETI
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-12-18
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2022-12-31
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 81314-201-01 WANCAREONEHAND ANTISEPTIC HAND Gel 5 mL in 1 PACKET GEL 5 1 81314-201-02 WANCAREONEHAND ANTISEPTIC HAND Gel 50 mL in 1 BOTTLE GEL 50 1 81314-201-03 WANCAREONEHAND ANTISEPTIC HAND Gel 100 mL in 1 BOTTLE GEL 100 1 81314-201-04 WANCAREONEHAND ANTISEPTIC HAND Gel 250 mL in 1 BOTTLE GEL 250 1 81314-201-05 WANCAREONEHAND ANTISEPTIC HAND Gel 500 mL in 1 BOTTLE GEL 500 1 81314-201-06 WANCAREONEHAND ANTISEPTIC HAND Gel 1000 mL in 1 BOTTLE GEL 1000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81314-201 WANCARE ONEHAND ANTISEPTIC HAND GEL (ETHYL ALCOHOL) GEL [KAF GRUP SAGLIK HIZMETLERI INSAAT SANAYI VE TICARET LIMITED SIRKETI] 1 Legacy NDC, 6 package rows 20210108_d08c8df3-a062-443b-b4fa-77ca5c686ea4.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 81314-201-03 81314020103 100 mL in 1 BOTTLE (81314-201-03) 100 ml 2020-12-18 0000-00-00 No No Current