LanoGuard

Product NDC
12090-0042
11-digit product format
120900042
Labeler code
12090
Product ID
12090-0042_597f599d-ec66-429f-b765-6be4f1b650b2
Type
HUMAN OTC DRUG
Nonproprietary name
LANOLIN
Dosage form
CREAM
Route
TOPICAL
Labeler
Summit Industries, Inc.
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2009-12-30
Marketing end
0000-00-00
Substance
LANOLIN
Active strength
370 mg/g
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
12090-0042-52019-11-27C16284748780-19855d018-e4a7-cd31-e053-dbdaa90ab51aLanoGuard Dry Skin Therapy Therapeutic Cream Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12090-0042-5LanoGuardDry Skin Therapy113 g in 1 TUBECREAM1131

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12090-0042LANOGUARD DRY SKIN THERAPY (LANOLIN) CREAM [SUMMIT INDUSTRIES, INC.]1Legacy NDC, 1 package rows20130322_949fc142-c7ba-4f73-b47a-418e079da3ae.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
746068lanolin 37 % Topical CreamPSN949fc142-c7ba-4f73-b47a-418e079da3ae1
746068lanolin 370 MG/ML Topical CreamSCD949fc142-c7ba-4f73-b47a-418e079da3ae1
746068lanolin 37 % Topical CreamSY949fc142-c7ba-4f73-b47a-418e079da3ae1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
12090-0042-512090004205113 g in 1 TUBE113 gHistorical