GOOD SENSE DAYTIME
- Product NDC
- 0113-7019
- 11-digit product format
- 001137019
- Labeler code
- 0113
- Product ID
- 0113-7019_27a7ef07-581c-4ba1-a259-a1e3ba9fa002
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-19
- Substance
- ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 325; 10 mg/1; mg/1
- Pharmacologic classes
- Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GOOD SENSE DAYTIME
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/1 |
| DEXTROMETHORPHAN HYDROBROMIDE | 10 mg/1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 0113-7019-53 | 00113701953 | 6 BLISTER PACK in 1 CARTON (0113-7019-53) / 2 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2026-06-19 | No | No | Current |
| 0113-7019-62 | 00113701962 | 12 BLISTER PACK in 1 CARTON (0113-7019-62) / 2 TABLET, FILM COATED in 1 BLISTER PACK | 12 blister pack | 2026-07-21 | No | No | Current |