Home NDC 81907-101 NasalGuard Antiseptic Topical Cool Menthol
Product NDC 81907-101
11-digit product format 819070101
Labeler code 81907
Product ID 81907-101_5a71fe2f-cad5-bdc5-e063-6294a90aefcb
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form GEL
Route TOPICAL
Labeler TRUTEK CORP.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-10-24
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/1000mg
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 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 81907-101 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 81907-101 81907-101-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 NasalGuard Antiseptic Topical Cool Menthol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 mg/1000mg
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 1098199 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 81907-101-01 NasalGuard Antiseptic Topical Cool Menthol 1 in 1 BOX GEL 1 9 81907-101-03 NasalGuard Antiseptic Topical Cool Menthol 3000 mg in 1 TUBE GEL 3000 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81907-101 NASALGUARD ANTISEPTIC TOPICAL COOL MENTHOL (BENZALKONIUM CHLORIDE) GEL [TRUTEK CORP.] 8 Current NDC, Legacy NDC, 2 package rows 20250117_e9fd3ef8-78ff-6c9f-e053-2a95a90a21a8.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 100 of 115 · 2,286 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 81907-101-01 81907010101 1 TUBE in 1 BOX (81907-101-01) / 3000 mg in 1 TUBE (81907-101-03) 1 tube 2024-02-01 No No Current 81907-101-03 81907010103 1 TUBE in 1 BOX (81907-101-03) > 3 g in 1 TUBE (81907-101-01) 1 tube 2022-02-14 0000-00-00 No No Current