Ultra Tuss is a Oral Syrup in the Human Otc Drug category. It is labeled and distributed by Ultra Seal Corporation. The primary component is Guaifenesin.
Product ID | 42213-160_0bab7cdc-aaeb-4649-83b0-17961b3a97f4 |
NDC | 42213-160 |
Product Type | Human Otc Drug |
Proprietary Name | Ultra Tuss |
Generic Name | Guaifenesin |
Dosage Form | Syrup |
Route of Administration | ORAL |
Marketing Start Date | 2012-06-19 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Ultra Seal Corporation |
Substance Name | GUAIFENESIN |
Active Ingredient Strength | 100 mg/5mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2012-06-19 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-06-19 |
Ingredient | Strength |
---|---|
GUAIFENESIN | 100 mg/5mL |
SPL SET ID: | f6f162ba-1c9b-436a-ba9e-fe49ac9a8e83 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
42213-160 | Ultra Tuss | Ultra Tuss |
0363-0288 | childrens chest congestion | Guaifenesin |
0113-0325 | Good Sense Mucus ER | Guaifenesin |
0113-2023 | good sense mucus er | guaifenesin |
0113-3650 | Good Sense Mucus ER | Guaifenesin |
0113-0061 | good sense tussin | Guaifenesin |
0121-0744 | GUAIFENESIN | GUAIFENESIN |
0121-1488 | GUAIFENESIN | GUAIFENESIN |
0121-1744 | GUAIFENESIN | GUAIFENESIN |
0121-2232 | GUAIFENESIN | GUAIFENESIN |
0363-0028 | Guaifenesin | Guaifenesin |
0363-0033 | Guaifenesin | Guaifenesin |
0363-0071 | Mucus | Guaifenesin |
0363-0074 | Mucus | Guaifenesin |
0363-0532 | Mucus Relief | Guaifenesin |
0363-0325 | mucus relief er | Guaifenesin |
0031-9303 | Robitussin Direct Chest Congestion | guaifenesin |
0031-8724 | Robitussin Mucus Plus Chest Congestion | Guaifenesin |
0113-2061 | tussin | Guaifenesin |
0363-0310 | wal tussin | Guaifenesin |