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