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Oticin
Oticin - 68436-115-10 - (Chloroxylenol / Pramoxine HCl)
Drug Information of Oticin
| Product NDC: | 68436-115 |
| Proprietary Name: | Oticin |
| Non Proprietary Name: | Chloroxylenol / Pramoxine HCl |
| Active Ingredient(s): | .01; .1 g/10mL; g/10mL & nbsp; Chloroxylenol / Pramoxine HCl |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oticin
| Product NDC: | 68436-115 |
| Labeler Name: | Teral, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091112 |
Package Information of Oticin
| Package NDC: | 68436-115-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 PACKAGE (68436-115-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of Oticin
| NDC Code | 68436-115-10 |
| Proprietary Name | Oticin |
| Package Description | 1 BOTTLE, DROPPER in 1 PACKAGE (68436-115-10) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 68436-115 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chloroxylenol / Pramoxine HCl |
| 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; PRAMOXINE HYDROCHLORIDE |
| Strength Number | .01; .1 |
| Strength Unit | g/10mL; g/10mL |
| Pharmaceutical Classes |
