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 |