Home
>
National Drug Code (NDC)
>
Rohto Ice
Rohto Ice - 75977-8143-1 - (hypromellose, tetrahydrozoline HCl, zinc sulfate)
Drug Information of Rohto Ice
| Product NDC: | 75977-8143 |
| Proprietary Name: | Rohto Ice |
| Non Proprietary Name: | hypromellose, tetrahydrozoline HCl, zinc sulfate |
| Active Ingredient(s): | 2; .5; 2.5 mg/mL; mg/mL; mg/mL & nbsp; hypromellose, tetrahydrozoline HCl, zinc sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rohto Ice
| Product NDC: | 75977-8143 |
| Labeler Name: | Rohto-Mentholatum (Vietnam) Co. Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110801 |
Package Information of Rohto Ice
| Package NDC: | 75977-8143-1 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (75977-8143-1) > 13 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Information of Rohto Ice
| NDC Code | 75977-8143-1 |
| Proprietary Name | Rohto Ice |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (75977-8143-1) > 13 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 75977-8143 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | hypromellose, tetrahydrozoline HCl, zinc sulfate |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rohto-Mentholatum (Vietnam) Co. Ltd. |
| Substance Name | HYPROMELLOSES; TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE |
| Strength Number | 2; .5; 2.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
