NDC 0067-8162 - Theraflu Flu Relief Maximum Strength Daytime Nighttime Combo Pack
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0067-8162
- Package NDCs from labels
- 0067-8162-01
- Manufacturer
- Haleon US Holdings LLC
- Effective date
- 2024-03-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Theraflu Flu Relief Max Daytime - Haleon US Holdings LLC | Haleon US Holdings LLC | 2024-03-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0067-8162-01 | Theraflu Flu Relief Maximum StrengthDaytime Nighttime Combo Pack | 20 in 1 BLISTER PACK | TABLET | 20 | 15 mg | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0067-8162 | THERAFLU FLU RELIEF MAXIMUM STRENGTH DAYTIME NIGHTTIME COMBO PACK (ACETAMINOPHEN, DEXTROMETHORPHAN HBR AND ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR) KIT [HALEON US HOLDINGS LLC] | 3 | Unmatched | 20240310_68d3e88a-d1be-410b-92a1-863903b3aa61.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.