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 |