| Product NDC: | 59088-856 |
| Proprietary Name: | Dynamic Skin Recovery SPF30 |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Active Ingredient(s): | 30; 75; 5; 5 uL/mL; uL/mL; uL/mL; uL/mL & nbsp; Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59088-856 |
| Labeler Name: | PureTek Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090301 |
| Package NDC: | 59088-856-04 |
| Package Description: | 50 mL in 1 BOTTLE (59088-856-04) |
| NDC Code | 59088-856-04 |
| Proprietary Name | Dynamic Skin Recovery SPF30 |
| Package Description | 50 mL in 1 BOTTLE (59088-856-04) |
| Product NDC | 59088-856 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PureTek Corporation |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 30; 75; 5; 5 |
| Strength Unit | uL/mL; uL/mL; uL/mL; uL/mL |
| Pharmaceutical Classes |