| Product NDC: | 10096-0258 |
| Proprietary Name: | superSHOCK |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | .525; .315 g/10.5g; g/10.5g & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10096-0258 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110419 |
| Package NDC: | 10096-0258-1 |
| Package Description: | 10.5 g in 1 VIAL (10096-0258-1) |
| NDC Code | 10096-0258-1 |
| Proprietary Name | superSHOCK |
| Package Description | 10.5 g in 1 VIAL (10096-0258-1) |
| Product NDC | 10096-0258 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110419 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | .525; .315 |
| Strength Unit | g/10.5g; g/10.5g |
| Pharmaceutical Classes |