Plus Advanced

Product NDC
73755-300
11-digit product format
737550300
Labeler code
73755
Product ID
73755-300_a9825bef-ead4-416b-e053-2a95a90a5ce0
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Brand Name Distributor LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73755-300-012021-07-23C16284748780-1c7ccaba7-1c38-fd44-e053-dadaa90aa01ba982dfca-ae1b-6f4f-e053-2995a90a7b74

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73755-300-01Plus Advanced3785 mL in 1 BOTTLE, PLASTICGEL37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73755-300PLUS ADVANCED (ALCOHOL) GEL [BRAND NAME DISTRIBUTOR LLC]1Legacy NDC, 1 package rows20200703_a982dfca-ae1b-6f4f-e053-2995a90a7b74.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSNa982dfca-ae1b-6f4f-e053-2995a90a7b741
581662ethanol 0.7 ML/ML Topical GelSCDa982dfca-ae1b-6f4f-e053-2995a90a7b741
581662ethanol 70 % Topical GelSYa982dfca-ae1b-6f4f-e053-2995a90a7b741
581662ethyl alcohol 70 % Topical GelSYa982dfca-ae1b-6f4f-e053-2995a90a7b741

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
73755-300-01737550300013785 mL in 1 BOTTLE, PLASTIC3785 mlHistorical