Home NDC 21749-704-16 Purell Advanced Refreshing
Product NDC 21749-704
Requested package NDC 21749-704-16
11-digit product format 217490704
Labeler code 21749
Product ID 21749-704_48373fc9-5f94-fd6d-e063-6294a90a1055
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 2012-03-15
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…
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 Advanced Refreshing
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21749-704-01 Purell Advanced Refreshing 29 mL in 1 BOTTLE GEL 29 19 21749-704-02 Purell Advanced Refreshing 59 mL in 1 BOTTLE GEL 59 19 21749-704-04 Purell Advanced Refreshing 118 mL in 1 BOTTLE GEL 118 19 21749-704-08 Purell Advanced Refreshing 236 mL in 1 BOTTLE GEL 236 19 21749-704-10 Purell Advanced Refreshing 295 mL in 1 PACKAGE GEL 295 19 21749-704-12 Purell Advanced Refreshing 354 mL in 1 BOTTLE GEL 354 19 21749-704-13 Purell Advanced Refreshing 372 mL in 1 PACKAGE GEL 372 19 21749-704-15 Purell Advanced Refreshing 1500 mL in 1 PACKAGE GEL 1500 19 21749-704-16 Purell Advanced Refreshing 473 mL in 1 PACKAGE GEL 473 19 21749-704-20 Purell Advanced Refreshing 2000 mL in 1 PACKAGE GEL 2000 19 21749-704-24 Purell Advanced Refreshing 710 mL in 1 PACKAGE GEL 710 19 21749-704-28 Purell Advanced Refreshing 828 mL in 1 PACKAGE GEL 828 19 21749-704-33 Purell Advanced Refreshing 1000 mL in 1 PACKAGE GEL 1000 19 21749-704-45 Purell Advanced Refreshing 450 mL in 1 PACKAGE GEL 450 19 21749-704-50 Purell Advanced Refreshing 15 mL in 1 PACKAGE GEL 15 19 21749-704-59 Purell Advanced Refreshing 591 mL in 1 PACKAGE GEL 591 19 21749-704-65 Purell Advanced Refreshing 192 mL in 1 PACKAGE GEL 192 19
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALCOHOL ACTIVE INGREDIENT 3K9958V90M PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 ALCOHOL ACTIVE MOIETY 3K9958V90M PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 .ALPHA.-TOCOPHEROL ACETATE, D- INACTIVE INGREDIENT A7E6112E4N PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 AMINOMETHYLPROPANOL INACTIVE INGREDIENT LU49E6626Q PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 CAPRYLYL GLYCOL INACTIVE INGREDIENT 00YIU5438U PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 ISOPROPYL ALCOHOL INACTIVE INGREDIENT ND2M416302 PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3 WATER INACTIVE INGREDIENT 059QF0KO0R PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21749-704 PURELL ADVANCED REFRESHING (ALCOHOL) GEL [GOJO INDUSTRIES, INC.] 18 Current NDC, Legacy NDC, 17 package rows 20241212_b1beadc4-5cf4-4e28-90cc-3f9fdc132a90.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 21749-704-16 21749070416 473 mL in 1 PACKAGE (21749-704-16) 473 ml 2020-04-27 0000-00-00 No No Current