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Vaniply - 45334-600-05 - (dimethicone)
Drug Information of Vaniply
| Product NDC: | 45334-600 |
| Proprietary Name: | Vaniply |
| Non Proprietary Name: | dimethicone |
| Active Ingredient(s): | 10 mg/g & nbsp; dimethicone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vaniply
| Product NDC: | 45334-600 |
| Labeler Name: | Pharmaceutical Specialties, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110224 |
Package Information of Vaniply
| Package NDC: | 45334-600-05 |
| Package Description: | 5 g in 1 TUBE (45334-600-05) |
NDC Information of Vaniply
| NDC Code | 45334-600-05 |
| Proprietary Name | Vaniply |
| Package Description | 5 g in 1 TUBE (45334-600-05) |
| Product NDC | 45334-600 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dimethicone |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110224 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Pharmaceutical Specialties, Inc. |
| Substance Name | DIMETHICONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
