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Nasal Relief
Nasal Relief - 0536-5005-72 - (Oxymetazoline Hydrochloride)
Drug Information of Nasal Relief
| Product NDC: | 0536-5005 |
| Proprietary Name: | Nasal Relief |
| Non Proprietary Name: | Oxymetazoline Hydrochloride |
| Active Ingredient(s): | .05 g/100mL & nbsp; Oxymetazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nasal Relief
| Product NDC: | 0536-5005 |
| Labeler Name: | Rugby Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121029 |
Package Information of Nasal Relief
| Package NDC: | 0536-5005-72 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (0536-5005-72) > 15 mL in 1 BOTTLE, SPRAY |
NDC Information of Nasal Relief
| NDC Code | 0536-5005-72 |
| Proprietary Name | Nasal Relief |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (0536-5005-72) > 15 mL in 1 BOTTLE, SPRAY |
| Product NDC | 0536-5005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline Hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20121029 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .05 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
