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Ultra Color Rich - 10096-0191-1 - (OCTINOXATE)

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Drug Information of Ultra Color Rich

Product NDC: 10096-0191
Proprietary Name: Ultra Color Rich
Non Proprietary Name: OCTINOXATE
Active Ingredient(s): 210    mg/3g & nbsp;   OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): LIPSTICK
Coding System: National Drug Codes(NDC)

Labeler Information of Ultra Color Rich

Product NDC: 10096-0191
Labeler Name: Avon Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20091229

Package Information of Ultra Color Rich

Package NDC: 10096-0191-1
Package Description: 3 g in 1 CASE (10096-0191-1)

NDC Information of Ultra Color Rich

NDC Code 10096-0191-1
Proprietary Name Ultra Color Rich
Package Description 3 g in 1 CASE (10096-0191-1)
Product NDC 10096-0191
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE
Dosage Form Name LIPSTICK
Route Name TOPICAL
Start Marketing Date 20091229
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Avon Products, Inc.
Substance Name OCTINOXATE
Strength Number 210
Strength Unit mg/3g
Pharmaceutical Classes

Complete Information of Ultra Color Rich


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