Adventure Hand Sanitizer

Product NDC
77371-021
11-digit product format
773710021
Labeler code
77371
Product ID
77371-021_e43ea66f-ed7e-4049-e053-2995a90a1861
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
SPRAY
Route
TOPICAL
Labeler
NICETY SOLUTIONS LLC
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-05-05
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77371-021-01Adventure Hand Sanitizer38 mL in 1 BOTTLE, SPRAYSPRAY383

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77371-021ADVENTURE HAND SANITIZER (ALCOHOL) SPRAY [NICETY SOLUTIONS LLC]3Legacy NDC, 1 package rows20220722_a4eff95a-212c-9e5d-e053-2995a90adacf.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1367692ethanol 60 % Topical SprayPSNa4eff95a-212c-9e5d-e053-2995a90adacf3
1367692ethanol 0.6 ML/ML Topical SpraySCDa4eff95a-212c-9e5d-e053-2995a90adacf3
1367692ethanol 60 % Topical SpraySYa4eff95a-212c-9e5d-e053-2995a90adacf3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
77371-021-017737100210138 mL in 1 BOTTLE, SPRAY (77371-021-01) 38 ml2020-05-050000-00-00NoNoCurrent