FDA.reportPublic FDA data

Lanolin 50%

Product NDC
87236-019
11-digit product format
872360019
Labeler code
87236
Product ID
87236-019_513a5bbf-c2d9-9a9a-e063-6394a90af64a
Type
HUMAN OTC DRUG
Nonproprietary name
Lanolin
Dosage form
CREAM
Route
TOPICAL
Labeler
Aldermed Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-01
Substance
LANOLIN
Active strength
50 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Lanolin 50%
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LANOLIN50 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7EV65EAW6H
Rxcui1038957

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87236-019-04Lanolin 50%113 g in 1 TUBECREAM1131

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038957lanolin 50 % Topical CreamPSN513a5bb2-7879-f007-e063-6394a90a94ff1
1038957lanolin 500 MG/ML Topical CreamSCD513a5bb2-7879-f007-e063-6394a90a94ff1
1038957lanolin 50 % Topical CreamSY513a5bb2-7879-f007-e063-6394a90a94ff1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87236-019-0487236001904113 g in 1 TUBE (87236-019-04) 113 g2025-12-01NoNoCurrent