Theochem Foaming Hand Sanitizer

Product NDC
68878-118
11-digit product format
688780118
Labeler code
68878
Product ID
68878-118_4c10210c-8cff-4931-a507-bb01e8d5003e
Type
HUMAN OTC DRUG
Nonproprietary name
FOAMING HAND SANTIZER
Dosage form
LIQUID
Route
TOPICAL
Labeler
Theochem Laboratories Inc
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2008-10-01
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 mg/mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68878-118-102019-11-27C16284748780-19855e2a2-4c86-60a7-e053-dbdaa90a05bdFoaming Hand Santizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68878-118-10Theochem Foaming Hand Sanitizer1250 mL in 1 BOTTLE, DISPENSINGLIQUID12501

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68878-118THEOCHEM FOAMING HAND SANITIZER (FOAMING HAND SANTIZER) LIQUID [THEOCHEM LABORATORIES INC]1Legacy NDC, 1 package rows20131218_3da40799-9a82-4a8d-b9ed-46e838952c48.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN3da40799-9a82-4a8d-b9ed-46e838952c481
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD3da40799-9a82-4a8d-b9ed-46e838952c481
1038799benzalkonium chloride 0.1 % Topical FoamSY3da40799-9a82-4a8d-b9ed-46e838952c481

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
68878-118-10688780118101250 mL in 1 BOTTLE, DISPENSING1250 mlHistorical