AMBI Soothing Hand sanitizer

Product NDC
73453-143
11-digit product format
734530143
Labeler code
73453
Product ID
73453-143_09751799-664e-ec58-e063-6394a90aea39
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
AMBI Enterprises, llc
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-05-20
Substance
ALCOHOL
Active strength
.7 mL/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
AMBI Soothing Hand sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL.7 mL/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui581662

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73453-143-04AMBI Soothing Hand sanitizer118 mL in 1 CYLINDERGEL1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73453-143AMBI SOOTHING HAND SANITIZER (ALCOHOL) GEL [AMBI ENTERPRISES, LLC]2Current NDC, Legacy NDC, 1 package rows20231106_229a2afd-9f33-42b9-916d-df1e787181f7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSN229a2afd-9f33-42b9-916d-df1e787181f72
581662ethanol 0.7 ML/ML Topical GelSCD229a2afd-9f33-42b9-916d-df1e787181f72
581662ethanol 70 % Topical GelSY229a2afd-9f33-42b9-916d-df1e787181f72
581662ethyl alcohol 70 % Topical GelSY229a2afd-9f33-42b9-916d-df1e787181f72

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73453-143-0473453014304118 mL in 1 CYLINDER (73453-143-04) 118 ml2020-05-200000-00-00NoNoCurrent