Product NDC: | 0067-2086 |
Proprietary Name: | 4 Way |
Non Proprietary Name: | Phenylephrine hydrochloride |
Active Ingredient(s): | .01 L/L & nbsp; Phenylephrine hydrochloride |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0067-2086 |
Labeler Name: | Novartis Consumer Health, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100101 |
Package NDC: | 0067-2086-15 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (0067-2086-15) > .037 L in 1 BOTTLE, SPRAY |
NDC Code | 0067-2086-15 |
Proprietary Name | 4 Way |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (0067-2086-15) > .037 L in 1 BOTTLE, SPRAY |
Product NDC | 0067-2086 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Phenylephrine hydrochloride |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20100101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Novartis Consumer Health, Inc. |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | .01 |
Strength Unit | L/L |
Pharmaceutical Classes |