| 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 |