Home NDC 81775-100-03 Antimicrobial Foaming Hand
Product NDC 81775-100
Requested package NDC 81775-100-03
11-digit product format 817750100
Labeler code 81775
Product ID 81775-100_2fbac9d4-5f01-0ce7-e063-6394a90a3573
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form SOAP
Route TOPICAL
Labeler Health Technology Professional Products, Inc
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-03-20
Substance BENZALKONIUM CHLORIDE
Active strength .0013 g/mL
NDC exclude flag No
Listing certified through 2026-12-31
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, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 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…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Antimicrobial Foaming Hand
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .0013 g/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 81775-100-01 Antimicrobial Foaming Hand 50.28 mL in 1 BOTTLE, PUMP SOAP 50.28 3 81775-100-02 Antimicrobial Foaming Hand 500 mL in 1 BOTTLE, PUMP SOAP 500 3 81775-100-03 Antimicrobial Foaming Hand 3785.4 mL in 1 BOTTLE SOAP 3785.4 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81775-100 ANTIMICROBIAL FOAMING HAND (BENZALKONIUM CHLORIDE) SOAP [HEALTH TECHNOLOGY PROFESSIONAL PRODUCTS, INC] 3 Current NDC, Legacy NDC, 3 package rows 20250313_dbca0970-88ca-04a4-e053-2995a90a68f2.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 81775-100-03 81775010003 3785.4 mL in 1 BOTTLE (81775-100-03) 3785.4 ml 2022-03-30 0000-00-00 No No Current