Docosanol

Product NDC
41163-724
11-digit product format
411630724
Labeler code
41163
Product ID
41163-724_c716eb17-fed9-4929-a185-424cb802280e
Type
HUMAN OTC DRUG
Nonproprietary name
Docosanol
Dosage form
CREAM
Route
TOPICAL
Labeler
United Natural Foods, Inc. dba UNFI
Application
ANDA208754
Marketing category
ANDA
Marketing start
2021-06-01
Substance
DOCOSANOL
Active strength
100 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Docosanol
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DOCOSANOL100 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9G1OE216XY
Rxcui797534

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-724-07Docosanol2 g in 1 TUBECREAM23
41163-724-07Docosanol1 in 1 PACKAGECREAM13

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
797534docosanol 10 % Topical CreamPSN7dd527af-878c-4150-86d0-69881b5e3f8f3
797534docosanol 100 MG/ML Topical CreamSCD7dd527af-878c-4150-86d0-69881b5e3f8f3
797534docosanol 10 % Topical CreamSY7dd527af-878c-4150-86d0-69881b5e3f8f3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41163-724-07411630724071 TUBE in 1 PACKAGE (41163-724-07) / 2 g in 1 TUBE1 tube2021-06-010000-00-00NoNoCurrent