CVS Foaming Hand Sanitizer

Product NDC
69842-584
11-digit product format
698420584
Labeler code
69842
Product ID
69842-584_90febb8c-1c79-4260-bbc7-39e2a4c2e9c3
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
CVS Health
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-01-01
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69842-584-012025-01-30C16284748780-12cef2736-a6e7-d83d-e063-dadaa90ab31fCVS Foaming Hand Sanitizer Antibacterial

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-584-01CVS Foaming Hand Sanitizer Antibacterial222 mL in 1 BOTTLE, DISPENSINGLIQUID2222

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-584CVS FOAMING HAND SANITIZER ANTIBACTERIAL (BENZALKONIUM CHLORIDE) LIQUID [CVS HEALTH]2Legacy NDC, 1 package rows20220127_90ad0d77-cc40-46f2-99ac-2d358aee6d01.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN90ad0d77-cc40-46f2-99ac-2d358aee6d012
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD90ad0d77-cc40-46f2-99ac-2d358aee6d012
1020365benzalkonium chloride 0.13 % Topical FoamSY90ad0d77-cc40-46f2-99ac-2d358aee6d012

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-584-0169842058401222 mL in 1 BOTTLE, DISPENSING (69842-584-01) 222 ml2015-01-010000-00-00NoNoCurrent