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Rohto
Rohto - 10742-8144-1 - (Hypromellose, Tetrahydrozoline hydrochloride)
Drug Information of Rohto
| Product NDC: | 10742-8144 |
| Proprietary Name: | Rohto |
| Non Proprietary Name: | Hypromellose, Tetrahydrozoline hydrochloride |
| Active Ingredient(s): | 3.5; .5 mg/mL; mg/mL & nbsp; Hypromellose, Tetrahydrozoline hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rohto
| Product NDC: | 10742-8144 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060824 |
Package Information of Rohto
| Package NDC: | 10742-8144-1 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8144-1) > 13 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Information of Rohto
| NDC Code | 10742-8144-1 |
| Proprietary Name | Rohto |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8144-1) > 13 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 10742-8144 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hypromellose, Tetrahydrozoline hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20060824 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | HYPROMELLOSES; TETRAHYDROZOLINE HYDROCHLORIDE |
| Strength Number | 3.5; .5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
