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KELO-COTE HC Anti-Itch Scar Treatment
KELO-COTE HC Anti-Itch Scar Treatment - 40101-001-00 - (HYDROCORTISONE ACETATE)
Drug Information of KELO-COTE HC Anti-Itch Scar Treatment
| Product NDC: | 40101-001 |
| Proprietary Name: | KELO-COTE HC Anti-Itch Scar Treatment |
| Non Proprietary Name: | HYDROCORTISONE ACETATE |
| Active Ingredient(s): | 1 g/100g & nbsp; HYDROCORTISONE ACETATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KELO-COTE HC Anti-Itch Scar Treatment
| Product NDC: | 40101-001 |
| Labeler Name: | Advanced Bio-Technologies, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120102 |
Package Information of KELO-COTE HC Anti-Itch Scar Treatment
| Package NDC: | 40101-001-00 |
| Package Description: | 1 TUBE in 1 CARTON (40101-001-00) > 10 g in 1 TUBE |
NDC Information of KELO-COTE HC Anti-Itch Scar Treatment
| NDC Code | 40101-001-00 |
| Proprietary Name | KELO-COTE HC Anti-Itch Scar Treatment |
| Package Description | 1 TUBE in 1 CARTON (40101-001-00) > 10 g in 1 TUBE |
| Product NDC | 40101-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROCORTISONE ACETATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120102 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Advanced Bio-Technologies, Inc |
| Substance Name | HYDROCORTISONE ACETATE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
