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DIMETHICONE and ZINC OXIDE
DIMETHICONE and ZINC OXIDE - 59779-082-02 - (DIMETHICONE and ZINC OXIDE)
Drug Information of DIMETHICONE and ZINC OXIDE
| Product NDC: | 59779-082 |
| Proprietary Name: | DIMETHICONE and ZINC OXIDE |
| Non Proprietary Name: | DIMETHICONE and ZINC OXIDE |
| Active Ingredient(s): | 10; 100 mg/g; mg/g & nbsp; DIMETHICONE and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIMETHICONE and ZINC OXIDE
| Product NDC: | 59779-082 |
| Labeler Name: | CVS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090601 |
Package Information of DIMETHICONE and ZINC OXIDE
| Package NDC: | 59779-082-02 |
| Package Description: | 113 g in 1 TUBE (59779-082-02) |
NDC Information of DIMETHICONE and ZINC OXIDE
| NDC Code | 59779-082-02 |
| Proprietary Name | DIMETHICONE and ZINC OXIDE |
| Package Description | 113 g in 1 TUBE (59779-082-02) |
| Product NDC | 59779-082 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIMETHICONE and ZINC OXIDE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS |
| Substance Name | DIMETHICONE; ZINC OXIDE |
| Strength Number | 10; 100 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
