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Peter Thomas Roth CC
Peter Thomas Roth CC - 65278-007-16 - (Titanium Dioxide and Zinc Oxide)
Drug Information of Peter Thomas Roth CC
| Product NDC: | 65278-007 |
| Proprietary Name: | Peter Thomas Roth CC |
| Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
| Active Ingredient(s): | 102.6; 57.6 mg/mL; mg/mL & nbsp; Titanium Dioxide and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Peter Thomas Roth CC
| Product NDC: | 65278-007 |
| Labeler Name: | June Jacobs Laboratories LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130222 |
Package Information of Peter Thomas Roth CC
| Package NDC: | 65278-007-16 |
| Package Description: | 15 mL in 1 TUBE (65278-007-16) |
NDC Information of Peter Thomas Roth CC
| NDC Code | 65278-007-16 |
| Proprietary Name | Peter Thomas Roth CC |
| Package Description | 15 mL in 1 TUBE (65278-007-16) |
| Product NDC | 65278-007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | June Jacobs Laboratories LLC |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 102.6; 57.6 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
