Home NDC 77371-023-01 Adventure Hand Sanitizer - Unscented 80%
Product NDC 77371-023
Requested package NDC 77371-023-01
11-digit product format 773710023
Labeler code 77371
Product ID 77371-023_49903f8e-a791-45c3-e063-6294a90a14e6
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler NICETY SOLUTIONS LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-05-05
Substance ALCOHOL
Active strength .8 mL/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 · 5 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 2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
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 Adventure Hand Sanitizer - Unscented 80%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL .8 mL/mL
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 1241663 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 77371-023-01 Adventure Hand Sanitizer - Unscented 80% 38 mL in 1 BOTTLE, SPRAY SPRAY 38 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 77371-023 ADVENTURE HAND SANITIZER - UNSCENTED 80% (ALCOHOL) SPRAY [NICETY SOLUTIONS LLC] 3 Current NDC, Legacy NDC, 1 package rows 20240620_a5077eb2-4adb-0680-e053-2995a90a2cef.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 77371-023-01 77371002301 38 mL in 1 BOTTLE, SPRAY (77371-023-01) 38 ml 2020-05-05 0000-00-00 No No Current