Home NDC 54860-415-01 Hand sanitizer 29ml
Product NDC 54860-415
Requested package NDC 54860-415-01
11-digit product format 548600415
Labeler code 54860
Product ID 54860-415_2d61fd7c-dc7b-095b-e063-6394a90a7709
Type HUMAN OTC DRUG
Nonproprietary name alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Shenzhen Lantern Scicence Co.,Ltd.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-22
Substance ALCOHOL
Active strength 65 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 54860-415 54860-415-01 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 54860-415 54860-415-01 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 54860-415 54860-415-01 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 Hand sanitizer 29ml
Brand name suffix 01
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 65 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 884783 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 54860-415-01 Hand sanitizer 29ml01 29 mL in 1 BOTTLE, PLASTIC LIQUID 29 34
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54860-415 HAND SANITIZER 29ML 01 (ALCOHOL) LIQUID [SHENZHEN LANTERN SCICENCE CO.,LTD.] 34 Current NDC, 1 package rows 20250207_037b4acb-49ca-bc0a-e063-6394a90a1fcc.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 9 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 Sample Exclude flag Status 54860-415-01 54860041501 29 mL in 1 BOTTLE, PLASTIC (54860-415-01) 29 ml 2023-08-23 Yes No Current