| Product NDC: | 10096-0178 |
| Proprietary Name: | Solutions |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE |
| Active Ingredient(s): | 20; 75; 50; 40 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10096-0178 |
| Labeler Name: | Avon Products, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130123 |
| Package NDC: | 10096-0178-2 |
| Package Description: | 1 JAR in 1 CARTON (10096-0178-2) > 50 mL in 1 JAR (10096-0178-1) |
| NDC Code | 10096-0178-2 |
| Proprietary Name | Solutions |
| Package Description | 1 JAR in 1 CARTON (10096-0178-2) > 50 mL in 1 JAR (10096-0178-1) |
| Product NDC | 10096-0178 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130123 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 20; 75; 50; 40 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |