| Product NDC: | 64760-215 |
| Proprietary Name: | Glytone Suncare block sunscreen |
| Non Proprietary Name: | octinoxate, octisalate, xinc oxide |
| Active Ingredient(s): | 9; 2.4; 9 mL/120mL; mL/120mL; mL/120mL & nbsp; octinoxate, octisalate, xinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64760-215 |
| Labeler Name: | Genesis Pharmaceutical |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100625 |
| Package NDC: | 64760-215-02 |
| Package Description: | 1 TUBE in 1 CARTON (64760-215-02) > 120 mL in 1 TUBE |
| NDC Code | 64760-215-02 |
| Proprietary Name | Glytone Suncare block sunscreen |
| Package Description | 1 TUBE in 1 CARTON (64760-215-02) > 120 mL in 1 TUBE |
| Product NDC | 64760-215 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, xinc oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100625 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Genesis Pharmaceutical |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 9; 2.4; 9 |
| Strength Unit | mL/120mL; mL/120mL; mL/120mL |
| Pharmaceutical Classes |