Nasal Decongestant PE Sinus Congestion Relief Non-Drowsy / Maximum Strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by H E B. The primary component is Phenylephrine Hydrochloride.
| Product ID | 37808-953_a7474871-180d-4e0f-87be-76f0e919df58 |
| NDC | 37808-953 |
| Product Type | Human Otc Drug |
| Proprietary Name | Nasal Decongestant PE Sinus Congestion Relief Non-Drowsy / Maximum Strength |
| Generic Name | Phenylephrine Hcl |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2005-01-14 |
| Marketing End Date | 2021-01-29 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | H E B |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 10 mg/1 |
| NDC Exclude Flag | N |
| Marketing Start Date | 2005-01-14 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-01-14 |
| Marketing End Date | 2021-01-29 |
| Ingredient | Strength |
|---|---|
| PHENYLEPHRINE HYDROCHLORIDE | 10 mg/1 |
| SPL SET ID: | 9177d4be-d53c-4a56-95d7-e08aaa03e4cd |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 37808-953 | Nasal Decongestant PE Sinus Congestion Relief Non-Drowsy / Maximum Strength | Nasal Decongestant PE Sinus Congestion Relief Non-Drowsy / Maximum Strength |
| 0363-4531 | Nasal Decongestant | Phenylephrine HCl |
| 30142-953 | Nasal Decongestant | Phenylephrine HCl |
| 33992-0453 | Nasal Decongestant | Phenylephrine HCl |
| 21130-453 | Nasal Decongestant PE | Phenylephrine HCl |
| 37808-453 | Nasal Decongestant PE | Phenylephrine HCl |
| 36800-704 | PE Sinus Congestion | Phenylephrine HCl |
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