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Sunscreen
Sunscreen - 29565-200-50 - (Zinc oxide)
Drug Information of Sunscreen
| Product NDC: | 29565-200 |
| Proprietary Name: | Sunscreen |
| Non Proprietary Name: | Zinc oxide |
| Active Ingredient(s): | 12.9 mL/52mL & nbsp; Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunscreen
| Product NDC: | 29565-200 |
| Labeler Name: | UV Natural International Pty Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060101 |
Package Information of Sunscreen
| Package NDC: | 29565-200-50 |
| Package Description: | 156 mL in 1 TUBE (29565-200-50) |
NDC Information of Sunscreen
| NDC Code | 29565-200-50 |
| Proprietary Name | Sunscreen |
| Package Description | 156 mL in 1 TUBE (29565-200-50) |
| Product NDC | 29565-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | UV Natural International Pty Ltd |
| Substance Name | ZINC OXIDE |
| Strength Number | 12.9 |
| Strength Unit | mL/52mL |
| Pharmaceutical Classes |
