Home NDC 69790-488 Antibacterial Hand Wash
Product NDC 69790-488
11-digit product format 697900488
Labeler code 69790
Product ID 69790-488_4b09a24b-e82c-d0ea-e063-6294a90a5ea9
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium chloride 0.13%
Dosage form LIQUID
Route TOPICAL
Labeler Uline
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-05-27
Substance BENZALKONIUM CHLORIDE
Active strength 1.313 mg/mL
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product 69790-488 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 69790-488 69790-488-08 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…
Additional Listing Data#
Finished product Yes
Brand name base Antibacterial Hand Wash
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.313 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1046593 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 69790-488-08 Antibacterial Hand Wash 3785 mL in 1 BOTTLE, PLASTIC LIQUID 3785 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69790-488 ANTIBACTERIAL HAND WASH (BENZALKONIUM CHLORIDE 0.13%) LIQUID [ULINE] 9 Current NDC, Legacy NDC, 1 package rows 20240929_9e7a97a0-f3dd-40cf-b25e-8ebb65693926.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 69790-488-08 69790048808 3785 mL in 1 BOTTLE, PLASTIC (69790-488-08) 3785 ml 2018-05-27 0000-00-00 No No Current