Home NDC 81314-101-03 WANCARE
Product NDC 81314-101
Requested package NDC 81314-101-03
11-digit product format 813140101
Labeler code 81314
Product ID 81314-101_6f60dd1c-c354-4181-a341-883647d4eb2c
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form SOLUTION
Route TOPICAL
Labeler KAF GRUP SAGLIK HIZMETLERI INSAAT SANAYI VE TICARET LIMITED SIRKETI
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-03-20
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 81314-101-01 WANCAREONEHAND HAND SANITIZER 50 mL in 1 BOTTLE SOLUTION 50 1 81314-101-02 WANCAREONEHAND HAND SANITIZER 100 mL in 1 BOTTLE SOLUTION 100 1 81314-101-03 WANCAREONEHAND HAND SANITIZER 250 mL in 1 BOTTLE SOLUTION 250 1 81314-101-04 WANCAREONEHAND HAND SANITIZER 500 mL in 1 BOTTLE SOLUTION 500 1 81314-101-05 WANCAREONEHAND HAND SANITIZER 1000 mL in 1 BOTTLE SOLUTION 1000 1 81314-101-06 WANCAREONEHAND HAND SANITIZER 5000 mL in 1 BOTTLE SOLUTION 5000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81314-101 WANCARE ONEHAND HAND SANITIZER (ETHYL ALCOHOL) SOLUTION [KAF GRUP SAGLIK HIZMETLERI INSAAT SANAYI VE TICARET LIMITED SIRKETI] 1 Legacy NDC, 6 package rows 20210108_cd7b4f7b-b28f-47e4-8ae1-5783b6847e8b.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 81314-101-03 81314010103 250 mL in 1 BOTTLE (81314-101-03) 250 ml 2020-03-20 0000-00-00 No No Current