| 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 |