| Product NDC: | 62802-144 |
| Proprietary Name: | Ocean Potion Quick Dry SPF 70 Sunscreen |
| Non Proprietary Name: | avobenzone, homosalate, oxybenzone,octisalate, octocrylene |
| Active Ingredient(s): | 2; 15; 5; 2; 6 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; avobenzone, homosalate, oxybenzone,octisalate, octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62802-144 |
| Labeler Name: | Sun & Skin Care Research, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120101 |
| Package NDC: | 62802-144-03 |
| Package Description: | 89 mL in 1 BOTTLE (62802-144-03) |
| NDC Code | 62802-144-03 |
| Proprietary Name | Ocean Potion Quick Dry SPF 70 Sunscreen |
| Package Description | 89 mL in 1 BOTTLE (62802-144-03) |
| Product NDC | 62802-144 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | avobenzone, homosalate, oxybenzone,octisalate, octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sun & Skin Care Research, Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 2; 15; 5; 2; 6 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |