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 |