| Product NDC: | 10742-8142 |
| Proprietary Name: | Rohto |
| Non Proprietary Name: | Naphazoline hydrochloride, Polysorbate 80 |
| Active Ingredient(s): | .12; 2 mg/mL; mg/mL & nbsp; Naphazoline hydrochloride, Polysorbate 80 |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10742-8142 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20010821 |
| Package NDC: | 10742-8142-1 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8142-1) > 13 mL in 1 BOTTLE, WITH APPLICATOR |
| NDC Code | 10742-8142-1 |
| Proprietary Name | Rohto |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8142-1) > 13 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 10742-8142 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naphazoline hydrochloride, Polysorbate 80 |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20010821 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE; POLYSORBATE 80 |
| Strength Number | .12; 2 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |