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NU-DERM PHYSICAL UV BLOCK
NU-DERM PHYSICAL UV BLOCK - 62032-102-36 - (ZINC OXIDE)
Drug Information of NU-DERM PHYSICAL UV BLOCK
| Product NDC: | 62032-102 |
| Proprietary Name: | NU-DERM PHYSICAL UV BLOCK |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 185 mg/g & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NU-DERM PHYSICAL UV BLOCK
| Product NDC: | 62032-102 |
| Labeler Name: | OMP, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040101 |
Package Information of NU-DERM PHYSICAL UV BLOCK
| Package NDC: | 62032-102-36 |
| Package Description: | 57 g in 1 BOTTLE, PLASTIC (62032-102-36) |
NDC Information of NU-DERM PHYSICAL UV BLOCK
| NDC Code | 62032-102-36 |
| Proprietary Name | NU-DERM PHYSICAL UV BLOCK |
| Package Description | 57 g in 1 BOTTLE, PLASTIC (62032-102-36) |
| Product NDC | 62032-102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20040101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OMP, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 185 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
