Home NDC 59555-903-11 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride
Product NDC 59555-903
Requested package NDC 59555-903-11
11-digit product format 595550903
Labeler code 59555
Product ID 59555-903_c4b804b7-76b9-4d09-aeb1-f0b99ea9f0e1
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LOTION
Route TOPICAL
Labeler R & R Lotion, Inc
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-12-21
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/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 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride
Listing expiration 2026-12-31 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 1046442 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59555-903-04 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 59 mL in 1 BOTTLE, DISPENSING LOTION 59 6 59555-903-07 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 118 mL in 1 BOTTLE, DISPENSING LOTION 118 6 59555-903-08 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 236 mL in 1 BOTTLE, DISPENSING LOTION 236 6 59555-903-09 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 473 mL in 1 BOTTLE, PUMP LOTION 473 6 59555-903-10 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 946 mL in 1 BOTTLE, PUMP LOTION 946 6 59555-903-11 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 3785 mL in 1 BOTTLE, PUMP LOTION 3785 6 59555-903-13 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 50 mL in 1 BOTTLE, PUMP LOTION 50 6 59555-903-14 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 88.7 mL in 1 BOTTLE, PUMP LOTION 88.7 6 59555-903-16 I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride 4 mL in 1 PACKET LOTION 4 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59555-903 I.C. SANITIZER AND RE-MOISTURIZER WITH BENZALKONIUM CHLORIDE (BENZALKONIUM CHLORIDE) LOTION [R & R LOTION, INC] 5 Current NDC, Legacy NDC, 9 package rows 20220510_cc5f24c8-fb85-49bd-8f55-4ec72fc0ffff.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 59555-903-11 59555090311 3785 mL in 1 BOTTLE, PUMP (59555-903-11) 3785 ml 2018-11-02 0000-00-00 No No Current