| Product NDC: | 76344-1001 |
| Proprietary Name: | Daily Defense Sunblock |
| Non Proprietary Name: | OCTINOXATE, ZINC OXIDE, ENZACAMENE, TITANIUM DIOXIDE, AMILOXATE, AVOBENZONE |
| Active Ingredient(s): | 2; .5; 3; 7.5; 2; 5 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; OCTINOXATE, ZINC OXIDE, ENZACAMENE, TITANIUM DIOXIDE, AMILOXATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76344-1001 |
| Labeler Name: | Humex,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130422 |
| Package NDC: | 76344-1001-2 |
| Package Description: | 1 TUBE in 1 BOX (76344-1001-2) > 50 mL in 1 TUBE (76344-1001-1) |
| NDC Code | 76344-1001-2 |
| Proprietary Name | Daily Defense Sunblock |
| Package Description | 1 TUBE in 1 BOX (76344-1001-2) > 50 mL in 1 TUBE (76344-1001-1) |
| Product NDC | 76344-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, ZINC OXIDE, ENZACAMENE, TITANIUM DIOXIDE, AMILOXATE, AVOBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130422 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Humex,Inc. |
| Substance Name | AMILOXATE; AVOBENZONE; ENZACAMENE; OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2; .5; 3; 7.5; 2; 5 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |