Home NDC 83986-118 Foaming Hand Sanitizer
Product NDC 83986-118
11-digit product format 839860118
Labeler code 83986
Product ID 83986-118_4cc3d5ce-f601-93a5-e063-6294a90a7296
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler UpLift Brands LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-29
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 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 · 1 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 83986-118 83986-118-44 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Additional Listing Data#
Finished product Yes
Brand name base Foaming Hand Sanitizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 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 1020365 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83986-118-44 Foaming Hand Sanitizer 532 mL in 1 BOTTLE, PLASTIC LIQUID 532 6 83986-118-45 Foaming Hand Sanitizer 1150 mL in 1 BOTTLE, PLASTIC LIQUID 1150 6 83986-118-86 Foaming Hand Sanitizer 1000 mL in 1 BOTTLE, PLASTIC LIQUID 1000 6 83986-118-96 Foaming Hand Sanitizer 221 mL in 1 BOTTLE, PLASTIC LIQUID 221 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83986-118 FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [UPLIFT BRANDS LLC] 4 Current NDC, 4 package rows 20250322_f8ca7e87-e5f1-4ef2-b389-02d318ccf78f.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 Sample Exclude flag Status 83986-118-44 83986011844 532 mL in 1 BOTTLE, PLASTIC 532 ml Historical 83986-118-45 83986011845 1150 mL in 1 BOTTLE, PLASTIC (83986-118-45) 1150 ml 2024-02-29 No No Current 83986-118-86 83986011886 1000 mL in 1 BOTTLE, PLASTIC (83986-118-86) 1000 ml 2024-02-29 No No Current 83986-118-96 83986011896 221 mL in 1 BOTTLE, PLASTIC (83986-118-96) 221 ml 2024-02-29 No No Current