Optase

Product NDC
72972-003
11-digit product format
729720003
Labeler code
72972
Product ID
72972-003_49a98c74-ad18-2e8d-e063-6394a90ac8cb
Type
HUMAN OTC DRUG
Nonproprietary name
white petrolatum, lanolin
Dosage form
OINTMENT
Route
OPHTHALMIC
Labeler
Scope Health Inc
Application
M018
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-05-05
Substance
LANOLIN; PETROLATUM
Active strength
.06; .9 g/g; g/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Optase
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LANOLIN.06 g/g
PETROLATUM.9 g/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7EV65EAW6H, 4T6H12BN9U

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72972-003-01Optase1 in 1 BOXOINTMENT16
72972-003-01Optase5 g in 1 TUBEOINTMENT56

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72972-003OPTASE (WHITE PETROLATUM, LANOLIN) OINTMENT [SCOPE HEALTH INC]5Current NDC, Legacy NDC, 2 package rows20241220_c1991caa-51b9-13d1-e053-2995a90a1293.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72972-003-01729720003011 TUBE in 1 BOX (72972-003-01) / 5 g in 1 TUBE1 tube2021-05-050000-00-00NoNoCurrent