Severe Cold and Flu Relief Daytime is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by The Kroger Co.. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride; Guaifenesin.
Product ID | 30142-716_3195382f-4f31-4eb7-b6b2-19036f33b31a |
NDC | 30142-716 |
Product Type | Human Otc Drug |
Proprietary Name | Severe Cold and Flu Relief Daytime |
Generic Name | Acetaminohpen, Dextromethorphan Hbr, Guaifenesin Phenylephrine Hcl |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2018-03-31 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | The Kroger Co. |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN |
Active Ingredient Strength | 650 mg/30mL; mg/30mL; mg/30mL; mg/30mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2018-03-31 |
Marketing End Date | 2025-03-31 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-03-31 |
Ingredient | Strength |
---|---|
ACETAMINOPHEN | 650 mg/30mL |
SPL SET ID: | cecd4f7f-5417-4e98-bc24-96803b6dfbe5 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
55319-415 | Severe Cold and Flu Relief Daytime | Severe Cold and Flu Relief Daytime |
55910-515 | Severe Cold and Flu Relief Daytime | Severe Cold and Flu Relief Daytime |
0363-4150 | Severe Cold and Flu Relief Daytime | Severe Cold and Flu Relief Daytime |
0363-7270 | Daytime Cold and Flu Relief | ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL |
30142-722 | Daytime Cold and Flu Relief | ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL |
30142-716 | Severe Cold and Flu Relief | ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL |