Product NDC: | 68436-110 |
Proprietary Name: | Oticin HC |
Non Proprietary Name: | Pramoxine HCl / Hydrocortisone / Chloroxylenol |
Active Ingredient(s): | .01; .1; .01 g/10mL; g/10mL; g/10mL & nbsp; Pramoxine HCl / Hydrocortisone / Chloroxylenol |
Administration Route(s): | AURICULAR (OTIC) |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68436-110 |
Labeler Name: | Teral, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20091112 |
Package NDC: | 68436-110-10 |
Package Description: | 1 BOTTLE, DROPPER in 1 PACKAGE (68436-110-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Code | 68436-110-10 |
Proprietary Name | Oticin HC |
Package Description | 1 BOTTLE, DROPPER in 1 PACKAGE (68436-110-10) > 10 mL in 1 BOTTLE, DROPPER |
Product NDC | 68436-110 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Pramoxine HCl / Hydrocortisone / Chloroxylenol |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | AURICULAR (OTIC) |
Start Marketing Date | 20091112 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Teral, Inc. |
Substance Name | CHLOROXYLENOL; HYDROCORTISONE; PRAMOXINE HYDROCHLORIDE |
Strength Number | .01; .1; .01 |
Strength Unit | g/10mL; g/10mL; g/10mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |