DailyMed label
Maxi-Tuss AC
DailyMed label · MCR American Pharmaceuticals, Inc. · version 1
Key facts
| Product | Maxi-Tuss AC |
|---|---|
| Labeler | MCR American Pharmaceuticals, Inc. |
| Document type | HUMAN OTC DRUG LABEL |
| Active ingredients | CODEINE PHOSPHATE, GUAIFENESIN |
| Active ingredient UNIIs | 495W7451VQ, GSL05Y1MN6 |
| Application number | part341 |
| Route | ORAL |
| DEA schedule | CV |
| NDC package codes | 58605-313-16 |
| Effective date | Jun 23, 2020 |
| Set ID | 4df08753-dc51-41f4-a8a7-11a76b318b02 |
At a glance
- 1–9 NDC package codes
- 1–9 Active ingredients
- 1–9 Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: