| Product NDC: | 64269-9903 |
| Proprietary Name: | Scarguard MD |
| Non Proprietary Name: | Hydrocortisone Silicone |
| Active Ingredient(s): | 5; 12 mg/mL; mL/100mL & nbsp; Hydrocortisone Silicone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64269-9903 |
| Labeler Name: | Scarguard Labs, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20011101 |
| Package NDC: | 64269-9903-8 |
| Package Description: | 30 mL in 1 BOTTLE, WITH APPLICATOR (64269-9903-8) |
| NDC Code | 64269-9903-8 |
| Proprietary Name | Scarguard MD |
| Package Description | 30 mL in 1 BOTTLE, WITH APPLICATOR (64269-9903-8) |
| Product NDC | 64269-9903 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone Silicone |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20011101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Scarguard Labs, LLC |
| Substance Name | HYDROCORTISONE; PHENYL TRIMETHICONE |
| Strength Number | 5; 12 |
| Strength Unit | mg/mL; mL/100mL |
| Pharmaceutical Classes |