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BabySpa
BabySpa - 42957-001-01 - (Zinc Oxide)
Drug Information of BabySpa
| Product NDC: | 42957-001 |
| Proprietary Name: | BabySpa |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 120 mg/mL & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BabySpa
| Product NDC: | 42957-001 |
| Labeler Name: | EXPRO3 LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120718 |
Package Information of BabySpa
| Package NDC: | 42957-001-01 |
| Package Description: | 100 mL in 1 TUBE (42957-001-01) |
NDC Information of BabySpa
| NDC Code | 42957-001-01 |
| Proprietary Name | BabySpa |
| Package Description | 100 mL in 1 TUBE (42957-001-01) |
| Product NDC | 42957-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120718 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | EXPRO3 LLC |
| Substance Name | ZINC OXIDE |
| Strength Number | 120 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
