Home NDC 71003-005-00 Hand Sanitizer
Product NDC 71003-005
Requested package NDC 71003-005-00
11-digit product format 710030005
Labeler code 71003
Product ID 71003-005_d605d77b-8dc4-33ec-e053-2a95a90a17c3
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form SPRAY
Route TOPICAL
Labeler Water Pure, Inc. d.b.a. Purity Products, Inc.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-08-12
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 64 mL/100mL
NDC exclude flag No
Listing certified through 2023-12-31
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 71003-005-00 Hand Sanitizer 60 mL in 1 BOTTLE, SPRAY SPRAY 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71003-005 HAND SANITIZER (ALCOHOL) SPRAY [WATER PURE, INC. D.B.A. PURITY PRODUCTS, INC.] 2 Legacy NDC, 1 package rows 20220121_acb0581c-606f-f89d-e053-2a95a90ad2eb.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71003-005-00 71003000500 60 mL in 1 BOTTLE, SPRAY (71003-005-00) 60 ml 2020-08-12 0000-00-00 No No Current