| Product NDC: | 49852-200 |
| Proprietary Name: | Suntan Lotion |
| Non Proprietary Name: | OCTINOXATE OXYBENZONE TITANIUM DIOXIDE |
| Active Ingredient(s): | 7; 6; 1 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE OXYBENZONE TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49852-200 |
| Labeler Name: | Tri-Coastal Design Company Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100228 |
| Package NDC: | 49852-200-60 |
| Package Description: | 60 mL in 1 TUBE (49852-200-60) |
| NDC Code | 49852-200-60 |
| Proprietary Name | Suntan Lotion |
| Package Description | 60 mL in 1 TUBE (49852-200-60) |
| Product NDC | 49852-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE OXYBENZONE TITANIUM DIOXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100228 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Tri-Coastal Design Company Inc. |
| Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 7; 6; 1 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |