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Rohto Hydra
Rohto Hydra - 10742-8148-1 - (Hydroxyethyl cellulose)
Drug Information of Rohto Hydra
| Product NDC: | 10742-8148 |
| Proprietary Name: | Rohto Hydra |
| Non Proprietary Name: | Hydroxyethyl cellulose |
| Active Ingredient(s): | 6 mg/mL & nbsp; Hydroxyethyl cellulose |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rohto Hydra
| Product NDC: | 10742-8148 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110103 |
Package Information of Rohto Hydra
| Package NDC: | 10742-8148-1 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (10742-8148-1) > 13 mL in 1 BOTTLE, DROPPER |
NDC Information of Rohto Hydra
| NDC Code | 10742-8148-1 |
| Proprietary Name | Rohto Hydra |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (10742-8148-1) > 13 mL in 1 BOTTLE, DROPPER |
| Product NDC | 10742-8148 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydroxyethyl cellulose |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110103 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) |
| Strength Number | 6 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
