CERTI-SINE is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Certified Safety Manufacturing. The primary component is Phenylephrine Hydrochloride.
| Product ID | 48083-330_262daeb0-6a7b-4fc6-b010-75b22c86c7f8 |
| NDC | 48083-330 |
| Product Type | Human Otc Drug |
| Proprietary Name | CERTI-SINE |
| Generic Name | Phenylephrine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2017-12-29 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Certified Safety Manufacturing |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 5 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2017-12-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-12-29 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-12-29 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-12-29 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-12-29 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-12-29 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-12-29 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-12-29 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| PHENYLEPHRINE HYDROCHLORIDE | 5 mg/1 |
| SPL SET ID: | 6825b90f-133c-457d-b75b-4a630c0a2030 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 48083-330 | CERTI-SINE | CERTI-SINE |
| 0067-2086 | 4 Way | Phenylephrine hydrochloride |
| 0113-7094 | basic care sinus pe | Phenylephrine Hydrochloride |
| 0363-0390 | ephrine nose | Phenylephrine hydrochloride |
| 0363-2023 | Ephrine Nose Drops | Phenylephrine hydrochloride |
| 0113-0094 | Good Sense Nasal Decongestant PE | Phenylephrine Hydrochloride |
| 0113-0648 | Good Sense Nasal Four | Phenylephrine hydrochloride |
| 0295-1217 | Little Remedies Decongestant Nose Drops | Phenylephrine Hydrochloride |
| 0363-0717 | nasal | Phenylephrine hydrochloride |
| 0295-1117 | Neo-Synephrine | Phenylephrine hydrochloride |
| 0295-1118 | Neo-Synephrine | Phenylephrine hydrochloride |
| 0295-1119 | Neo-Synephrine | Phenylephrine hydrochloride |
| 0225-0800 | Neo-Synephrine Mild | PHENYLEPHRINE HYDROCHLORIDE |
| 0225-0805 | Neo-Synephrine Regular | PHENYLEPHRINE HYDROCHLORIDE |
| 0225-0810 | Neo-Synephrine Regular | PHENYLEPHRINE HYDROCHLORIDE |
| 0363-0394 | phenylephrine hydrochloride | phenylephrine hydrochloride |
| 0404-9931 | Phenylephrine Hydrochloride | Phenylephrine Hydrochloride |
| 0641-6142 | Phenylephrine Hydrochloride | Phenylephrine Hydrochloride |
| 0641-6188 | Phenylephrine Hydrochloride | Phenylephrine Hydrochloride |
| 0641-6189 | Phenylephrine Hydrochloride | Phenylephrine Hydrochloride |
| 0641-6229 | Phenylephrine Hydrochloride | Phenylephrine Hydrochloride |
| 0781-3422 | Phenylephrine Hydrochloride | Phenylephrine Hydrochloride |
| 0781-3458 | Phenylephrine Hydrochloride | Phenylephrine Hydrochloride |
| 0113-2004 | sinus PE | Phenylephrine Hydrochloride |
| 0363-0648 | Wal Four | Phenylephrine hydrochloride |