Biosilk

Product NDC
73740-4040
11-digit product format
737404040
Labeler code
73740
Product ID
73740-4040_a22d11ea-e391-d9a4-e053-2a95a90acd3a
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
SOAP
Route
CUTANEOUS
Labeler
Farouk Systems, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-03-31
Marketing end
0000-00-00
Substance
BENZALKONIUM
Active strength
0 g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73740-4040-1Biosilk340 g in 1 BOTTLE, PUMPSOAP3401
73740-4040-5Biosilk739 g in 1 BOTTLE, PUMPSOAP7391
73740-4040-6Biosilk163 g in 1 BOTTLE, PUMPSOAP1631

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73740-4040BIOSILK (BENZALKONIUM CHLORIDE) SOAP [FAROUK SYSTEMS, INC.]1Legacy NDC, 3 package rows20200402_a22d11ea-e390-d9a4-e053-2a95a90acd3a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSNa22d11ea-e390-d9a4-e053-2a95a90acd3a1
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCDa22d11ea-e390-d9a4-e053-2a95a90acd3a1
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSYa22d11ea-e390-d9a4-e053-2a95a90acd3a1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73740-4040-173740404001340 g in 1 BOTTLE, PUMP (73740-4040-1) 340 g2020-03-310000-00-00NoNoCurrent
73740-4040-573740404005739 g in 1 BOTTLE, PUMP (73740-4040-5) 739 g2020-03-310000-00-00NoNoCurrent
73740-4040-673740404006163 g in 1 BOTTLE, PUMP (73740-4040-6) 163 g2020-03-310000-00-00NoNoCurrent