Lincoln

Product NDC
69636-3045
11-digit product format
696363045
Labeler code
69636
Product ID
69636-3045_45c37f14-ce77-523c-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
white petrolatum
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Lincoln Pharmaceuticals Ltd.
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-01-10
Marketing end
0000-00-00
Substance
PETROLATUM
Active strength
76 g/100g
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69636-3045-2Lincoln5 g in 1 PACKETOINTMENT51
69636-3045-3Lincoln28.3 g in 1 TUBEOINTMENT28.31
69636-3045-4Lincoln113 g in 1 TUBEOINTMENT1131
69636-3045-5Lincoln425 g in 1 JAROINTMENT4251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69636-3045LINCOLN (WHITE PETROLATUM) OINTMENT [LINCOLN PHARMACEUTICALS LTD.]1Legacy NDC, 4 package rows20170111_45c37f14-ce76-523c-e054-00144ff88e88.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049072petrolatum 76 % Topical OintmentPSN45c37f14-ce76-523c-e054-00144ff88e881
1049072petrolatum 0.76 MG/MG Topical OintmentSCD45c37f14-ce76-523c-e054-00144ff88e881
1049072petrolatum 76 % Topical OintmentSY45c37f14-ce76-523c-e054-00144ff88e881

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69636-3045-2696363045025 g in 1 PACKET5 gHistorical
69636-3045-36963630450328.3 g in 1 TUBE28.3 gHistorical
69636-3045-469636304504113 g in 1 TUBE113 gHistorical
69636-3045-569636304505425 g in 1 JAR425 gHistorical