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: | 62802-144-08 |
Package Description: | 237 mL in 1 BOTTLE (62802-144-08) |
NDC Code | 62802-144-08 |
Proprietary Name | Ocean Potion Quick Dry SPF 70 Sunscreen |
Package Description | 237 mL in 1 BOTTLE (62802-144-08) |
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 |