| Product NDC: | 12027-103 |
| Proprietary Name: | wet n wild |
| Non Proprietary Name: | OCTINOXATE OXYBENZONE |
| Active Ingredient(s): | 5; 1.5 g/100g; g/100g & nbsp; OCTINOXATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 12027-103 |
| Labeler Name: | Markwins Beauty Products, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111201 |
| Package NDC: | 12027-103-46 |
| Package Description: | 13 g in 1 CONTAINER (12027-103-46) |
| NDC Code | 12027-103-46 |
| Proprietary Name | wet n wild |
| Package Description | 13 g in 1 CONTAINER (12027-103-46) |
| Product NDC | 12027-103 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE OXYBENZONE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Markwins Beauty Products, Inc |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 5; 1.5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |