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Carlesta
Carlesta - 0713-0623-32 - (Dimethicone, Zinc Oxide)
Drug Information of Carlesta
| Product NDC: | 0713-0623 |
| Proprietary Name: | Carlesta |
| Non Proprietary Name: | Dimethicone, Zinc Oxide |
| Active Ingredient(s): | 20; 260 mg/g; mg/g & nbsp; Dimethicone, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carlesta
| Product NDC: | 0713-0623 |
| Labeler Name: | G&W Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19990908 |
Package Information of Carlesta
| Package NDC: | 0713-0623-32 |
| Package Description: | 56.8 g in 1 TUBE (0713-0623-32) |
NDC Information of Carlesta
| NDC Code | 0713-0623-32 |
| Proprietary Name | Carlesta |
| Package Description | 56.8 g in 1 TUBE (0713-0623-32) |
| Product NDC | 0713-0623 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dimethicone, Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19990908 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | G&W Laboratories, Inc. |
| Substance Name | DIMETHICONE; ZINC OXIDE |
| Strength Number | 20; 260 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
