ultra color absolute

Product NDC
10096-0325
11-digit product format
100960325
Labeler code
10096
Product ID
10096-0325_00b51523-cb2d-4242-aae7-345da33161a3
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate
Dosage form
LIPSTICK
Route
TOPICAL
Labeler
New Avon LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-12-19
Marketing end
0000-00-00
Substance
OCTINOXATE
Active strength
75 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
10096-0325-22020-01-31C16284748780-19d75b9d0-e230-f424-e053-dadaa90a57ce91e56b45-d96d-4a03-baee-043af451b68f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0325-1ultra color absolute3 g in 1 PACKAGELIPSTICK32
10096-0325-2ultra color absolute1 in 1 CARTONLIPSTICK12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD51ULTRA COLOR ABSOLUTE (OCTINOXATE) LIPSTICK [AVON PRODUCTS, INC]1
OCTINOXATEACTIVE MOIETY4Y5P7MUD51ULTRA COLOR ABSOLUTE (OCTINOXATE) LIPSTICK [AVON PRODUCTS, INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0325ULTRA COLOR ABSOLUTE (OCTINOXATE) LIPSTICK [NEW AVON LLC]2Legacy NDC, 2 package rows20160303_91e56b45-d96d-4a03-baee-043af451b68f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
10096-0325-1100960325013 g in 1 PACKAGE3 gHistorical
10096-0325-2100960325021 in 1 CARTONHistorical