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mark. For Gooness Face - 10096-0144-2 - (Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone)

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Drug Information of mark. For Gooness Face

Product NDC: 10096-0144
Proprietary Name: mark. For Gooness Face
Non Proprietary Name: Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone
Active Ingredient(s): 30; 80; 75; 50; 50    mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of mark. For Gooness Face

Product NDC: 10096-0144
Labeler Name: Avon Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130308

Package Information of mark. For Gooness Face

Package NDC: 10096-0144-2
Package Description: 1 JAR in 1 CARTON (10096-0144-2) > 50 mL in 1 JAR (10096-0144-1)

NDC Information of mark. For Gooness Face

NDC Code 10096-0144-2
Proprietary Name mark. For Gooness Face
Package Description 1 JAR in 1 CARTON (10096-0144-2) > 50 mL in 1 JAR (10096-0144-1)
Product NDC 10096-0144
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20130308
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Avon Products, Inc.
Substance Name AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 30; 80; 75; 50; 50
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of mark. For Gooness Face


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