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Rx Act nasal four
Rx Act nasal four - 37808-648-10 - (Phenylephrine hydrochloride)
Drug Information of Rx Act nasal four
| Product NDC: | 37808-648 |
| Proprietary Name: | Rx Act nasal four |
| Non Proprietary Name: | Phenylephrine hydrochloride |
| Active Ingredient(s): | 1 g/100mL & nbsp; Phenylephrine hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rx Act nasal four
| Product NDC: | 37808-648 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100924 |
Package Information of Rx Act nasal four
| Package NDC: | 37808-648-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-648-10) > 30 mL in 1 BOTTLE |
NDC Information of Rx Act nasal four
| NDC Code | 37808-648-10 |
| Proprietary Name | Rx Act nasal four |
| Package Description | 1 BOTTLE in 1 CARTON (37808-648-10) > 30 mL in 1 BOTTLE |
| Product NDC | 37808-648 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20100924 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
