Medicated First Aid

Product NDC
50804-773
11-digit product format
508040773
Labeler code
50804
Product ID
50804-773_91db2f40-c959-45e7-9af8-3ed02c1bb301
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride 0.10% Benzocaine 20.00%
Dosage form
SPRAY
Route
TOPICAL
Labeler
Good Sense
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-07-31
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE; BENZOCAINE
Active strength
0 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50804-773-032020-01-31C16284748780-19d75b9d0-25b4-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-773-03Medicated First AidGood Sense85 g in 1 CANSPRAY851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-773MEDICATED FIRST AID GOOD SENSE (BENZALKONIUM CHLORIDE 0.10% BENZOCAINE 20.00%) SPRAY [GOOD SENSE]1Legacy NDC, 1 package rows20180607_a0b8c362-c0f1-4ff5-b40e-23f5d822fb98.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2043455benzalkonium chloride 0.1 % / benzocaine 20 % Topical SprayPSNa0b8c362-c0f1-4ff5-b40e-23f5d822fb981
2043455benzalkonium chloride 1 MG/ML / benzocaine 200 MG/ML Topical SpraySCDa0b8c362-c0f1-4ff5-b40e-23f5d822fb981
2043455benzalkonium Cl 0.1 % / benzocaine 20 % Topical SpraySYa0b8c362-c0f1-4ff5-b40e-23f5d822fb981

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
50804-773-035080407730385 g in 1 CAN85 gHistorical