Home NDC 21749-717-10 PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel
Product NDC 21749-717
Requested package NDC 21749-717-10
11-digit product format 217490717
Labeler code 21749
Product ID 21749-717_46563bd7-3b3d-0ec2-e063-6394a90a9404
Type HUMAN OTC DRUG
Nonproprietary name alcohol
Dosage form GEL
Route TOPICAL
Labeler GOJO Industries, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-10-15
Marketing end 2027-04-12
Substance ALCOHOL
Active strength .7 mL/mL
NDC exclude flag No
Current FDA listing Yes 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 · 9 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…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL .7 mL/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 581662 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21749-717-08 PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel 236 mL in 1 PACKAGE GEL 236 4 21749-717-10 PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel 1000 mL in 1 PACKAGE GEL 1000 4 21749-717-12 PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel 354 mL in 1 PACKAGE GEL 354 4 21749-717-20 PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel 2000 mL in 1 PACKAGE GEL 2000 4 21749-717-89 PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel 1200 mL in 1 PACKAGE GEL 1200 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21749-717 PURELL PROFESSIONAL ADVANCED HAND SANITIZER FRAGRANCE FREE GEL (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 Current NDC, Legacy NDC, 5 package rows 20241208_4952bb21-fefa-4ae1-8e1a-feb412ce100c.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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 21749-717-10 21749071710 1000 mL in 1 PACKAGE (21749-717-10) 1000 ml 2017-10-15 0000-00-00 No No Current