| Product NDC: | 75885-010 |
| Proprietary Name: | PUTTO ATO SECRET UV FACE |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 1.34; 2.7 mL/80mL; mL/80mL & nbsp; ZINC OXIDE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75885-010 |
| Labeler Name: | AGABANG & COMPANY |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100401 |
| Package NDC: | 75885-010-01 |
| Package Description: | 80 mL in 1 CARTON (75885-010-01) |
| NDC Code | 75885-010-01 |
| Proprietary Name | PUTTO ATO SECRET UV FACE |
| Package Description | 80 mL in 1 CARTON (75885-010-01) |
| Product NDC | 75885-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | AGABANG & COMPANY |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 1.34; 2.7 |
| Strength Unit | mL/80mL; mL/80mL |
| Pharmaceutical Classes |