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Rohto Arctic
Rohto Arctic - 75977-8144-1 - (Hypromellose, Tetrahydrozoline hydrochloride)
Drug Information of Rohto Arctic
| Product NDC: | 75977-8144 |
| Proprietary Name: | Rohto Arctic |
| 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 Arctic
| Product NDC: | 75977-8144 |
| Labeler Name: | Rohto-Mentholatum (Vietnam) Co. Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120301 |
Package Information of Rohto Arctic
| Package NDC: | 75977-8144-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (75977-8144-1) > 13 mL in 1 BOTTLE |
NDC Information of Rohto Arctic
| NDC Code | 75977-8144-1 |
| Proprietary Name | Rohto Arctic |
| Package Description | 1 BOTTLE in 1 CARTON (75977-8144-1) > 13 mL in 1 BOTTLE |
| Product NDC | 75977-8144 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hypromellose, Tetrahydrozoline hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rohto-Mentholatum (Vietnam) Co. Ltd. |
| Substance Name | HYPROMELLOSE 2208 (100 MPA.S); TETRAHYDROZOLINE HYDROCHLORIDE |
| Strength Number | 3.5; .5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
