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rx act nasal decongestant pe
rx act nasal decongestant pe - 37808-094-23 - (Phenylephrine Hydrochloride)
Drug Information of rx act nasal decongestant pe
| Product NDC: | 37808-094 |
| Proprietary Name: | rx act nasal decongestant pe |
| Non Proprietary Name: | Phenylephrine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of rx act nasal decongestant pe
| Product NDC: | 37808-094 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20050607 |
Package Information of rx act nasal decongestant pe
| Package NDC: | 37808-094-23 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (37808-094-23) > 18 TABLET in 1 BLISTER PACK |
NDC Information of rx act nasal decongestant pe
| NDC Code | 37808-094-23 |
| Proprietary Name | rx act nasal decongestant pe |
| Package Description | 4 BLISTER PACK in 1 CARTON (37808-094-23) > 18 TABLET in 1 BLISTER PACK |
| Product NDC | 37808-094 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050607 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
