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Kendall Soothing
Kendall Soothing - 28851-695-02 - (Zinc Oxide)
Drug Information of Kendall Soothing
| Product NDC: | 28851-695 |
| Proprietary Name: | Kendall Soothing |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 10 mL/100mL & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kendall Soothing
| Product NDC: | 28851-695 |
| Labeler Name: | Covidien Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110422 |
Package Information of Kendall Soothing
| Package NDC: | 28851-695-02 |
| Package Description: | 118 mL in 1 TUBE (28851-695-02) |
NDC Information of Kendall Soothing
| NDC Code | 28851-695-02 |
| Proprietary Name | Kendall Soothing |
| Package Description | 118 mL in 1 TUBE (28851-695-02) |
| Product NDC | 28851-695 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110422 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Covidien Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 10 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
