Home NDC 55910-969 Moisturizing Antibacterial
Product NDC 55910-969
11-digit product format 559100969
Labeler code 55910
Product ID 55910-969_4c10db5e-59c4-dde2-e063-6294a90af0f4
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium chloride 0.13%
Dosage form SOAP
Route TOPICAL
Labeler Old East Main Co.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-10-12
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 g/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 · 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…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…
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 Moisturizing Antibacterial
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55910-969-68 Moisturizing Antibacterial 1656 mL in 1 BOTTLE, PLASTIC SOAP 1656 6 55910-969-81 Moisturizing Antibacterial 332 mL in 1 BOTTLE, PUMP SOAP 332 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-969 MOISTURIZING ANTIBACTERIAL (BENZALKONIUM CHLORIDE 0.13%) SOAP [OLD EAST MAIN CO.] 4 Current NDC, Legacy NDC, 2 package rows 20241013_122154ea-bdb3-4e71-bfd5-f1f28d75fb2e.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 55910-969-68 55910096968 1656 mL in 1 BOTTLE, PLASTIC (55910-969-68) 1656 ml 2021-10-12 0000-00-00 No No Current 55910-969-81 55910096981 332 mL in 1 BOTTLE, PUMP (55910-969-81) 332 ml 2021-10-12 0000-00-00 No No Current