SUDAFED PE DAY PLUS NIGHT SINUS CONGESTION is a Kit in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is .
Product ID | 50580-736_3631044f-259d-4822-9368-6a3eb7f5ce30 |
NDC | 50580-736 |
Product Type | Human Otc Drug |
Proprietary Name | SUDAFED PE DAY PLUS NIGHT SINUS CONGESTION |
Generic Name | Diphenhydramine Hydrochloride And Phenylephrine Hydrochloride |
Dosage Form | Kit |
Marketing Start Date | 2017-06-26 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2017-06-26 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-06-26 |
SPL SET ID: | 36513fd5-a7bd-40ef-b396-5f92e7ea0b2c |
Manufacturer | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
50580-736 | SUDAFED PE DAY PLUS NIGHT SINUS CONGESTION | Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride |
50580-415 | Benadryl Allergy Plus Congestion | Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride |
50580-341 | Childrens Benadryl Allergy Plus Congestion | Diphenhydramine hydrochloride and Phenylephrine hydrochloride |
80070-340 | Dimetapp | DIPHENHYDRAMINE HYDROCHLORIDE and PHENYLEPHRINE HYDROCHLORIDE |
45014-154 | Nite Time Cold and Cough | Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride |
45014-159 | Nite Time Cold and Cough | Diphenhydramine Hydrochloride and Phenylephrine Hydrochloride |
50580-239 | SUDAFED PE SINUS CONGESTION | diphenhydramine hydrochloride and phenylephrine hydrochloride |