Dial Complete Spring Water FHW

Product NDC
50663-242
11-digit product format
506630242
Labeler code
50663
Product ID
50663-242_a37e57c5-7bcc-14d7-e053-2a95a90a16de
Type
HUMAN OTC DRUG
Nonproprietary name
Dial Complete Spring Water FHW
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Zotos International Inc
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-05-01
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/100mL
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
50663-242-022022-01-28C16284748780-1d6a99b39-d854-a426-e053-dadaa90af4c2a37e57c5-7bcb-14d7-e053-2a95a90a16de

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50663-242-02Dial Complete Spring Water FHW221 mL in 1 BOTTLE, DISPENSINGSOLUTION2211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50663-242DIAL COMPLETE SPRING WATER FHW SOLUTION [ZOTOS INTERNATIONAL INC]1Legacy NDC, 1 package rows20200501_a37e57c5-7bcb-14d7-e053-2a95a90a16de.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSNa37e57c5-7bcb-14d7-e053-2a95a90a16de1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCDa37e57c5-7bcb-14d7-e053-2a95a90a16de1
1049254benzalkonium chloride 0.13 % Topical SolutionSYa37e57c5-7bcb-14d7-e053-2a95a90a16de1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50663-242-0250663024202221 mL in 1 BOTTLE, DISPENSING (50663-242-02) 221 ml2020-05-010000-00-00NoNoCurrent