Home NDC 66949-119 Zep Fuzion Instant Hand Sanitizer
Product NDC 66949-119
11-digit product format 669490119
Labeler code 66949
Product ID 66949-119_46de5f99-ebe7-c5ae-e063-6394a90a1bbb
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Zep Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-11-02
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Zep Fuzion Instant Hand Sanitizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66949-119-16 Zep Fuzion Instant Hand Sanitizer 4800 mL in 1 CASE LIQUID 4800 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66949-119 ZEP FUZION INSTANT HAND SANITIZER (ALCOHOL) LIQUID [ZEP INC.] 5 Current NDC, Legacy NDC, 1 package rows 20241120_b43c5701-22ee-1de4-e053-2995a90a8f64.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 66949-119-16 66949011916 4800 mL in 1 CASE (66949-119-16) 4800 ml 2020-11-02 0000-00-00 No No Current