| Product NDC: | 59663-120 |
| Proprietary Name: | Planet Sun SPF 30 |
| Non Proprietary Name: | OCTINOXATE, ZINC OXIDE |
| Active Ingredient(s): | 75; 100 mg/mL; mg/mL & nbsp; OCTINOXATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59663-120 |
| Labeler Name: | Shine & Pretty (USA), Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130301 |
| Package NDC: | 59663-120-04 |
| Package Description: | 120 mL in 1 TUBE (59663-120-04) |
| NDC Code | 59663-120-04 |
| Proprietary Name | Planet Sun SPF 30 |
| Package Description | 120 mL in 1 TUBE (59663-120-04) |
| Product NDC | 59663-120 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Shine & Pretty (USA), Corp. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 100 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |