Home NDC 78280-302-02 KeriCure Hand Sanitizer
Product NDC 78280-302
Requested package NDC 78280-302-02
11-digit product format 782800302
Labeler code 78280
Product ID 78280-302_6d220d4b-a2a9-488c-b38f-360a4e3b57ff
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler Kericure Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-04-10
Substance ALCOHOL
Active strength 70 mL/100mL
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 · 3 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 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 78280-302 78280-302-02 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 78280-302 78280-302-02 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 78280-302 78280-302-02 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 KeriCure Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1041849 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 78280-302-01 KeriCure Hand Sanitizer 28 mL in 1 BOTTLE, SPRAY SPRAY 28 3 78280-302-02 KeriCure Hand Sanitizer 55 mL in 1 BOTTLE, SPRAY SPRAY 55 3 78280-302-04 KeriCure Hand Sanitizer 115 mL in 1 BOTTLE, SPRAY SPRAY 115 3 78280-302-08 KeriCure Hand Sanitizer 230 mL in 1 BOTTLE, SPRAY SPRAY 230 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 78280-302 KERICURE HAND SANITIZER (ALCOHOL) SPRAY [KERICURE INC.] 3 Current NDC, Legacy NDC, 4 package rows 20250202_de516d2e-9c16-4bd2-b4c2-7e2f9fd26442.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 78280-302-02 78280030202 55 mL in 1 BOTTLE, SPRAY (78280-302-02) 55 ml 2020-04-10 0000-00-00 No No Current