Theraflu Severe Cold relief Nighttime
NDC 0067-6801, Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride, powder, from Haleon US Holdings LLC.
- Product NDC
- 0067-6801
- Status
- Listed
- Labeler
- Haleon US Holdings LLC
- Dosage form
- POWDER
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M012
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0067-6801 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN500 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1
- PHENYLEPHRINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA]; Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]; alpha-1 Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0067-6801-02 | 00067680102 | 6 POWDER in 1 CARTON (0067-6801-02) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 0067-6801 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0067-6801 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0067-6801. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.