Vicks DayQuil Severe Cold and Flu
NDC 37000-810, Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, solution, from The Procter & Gamble Manufacturing Company.
- Product NDC
- 37000-810
- Status
- Listed
- Labeler
- The Procter & Gamble Manufacturing Company
- Dosage form
- SOLUTION
- 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/37000-810 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN325 mg/15mL
- DEXTROMETHORPHAN HYDROBROMIDE10 mg/15mL
- GUAIFENESIN200 mg/15mL
- PHENYLEPHRINE HYDROCHLORIDE5 mg/15mL
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA]; Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]; Sigma-1 Agonist [EPC]; Sigma-1 Receptor Agonists [MoA]; Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]; Uncompetitive NMDA Receptor Antagonists [MoA]; alpha-1 Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 37000-810-01 | 37000081001 | 30 mL in 1 BOTTLE, PLASTIC (37000-810-01) |
| 37000-810-04 | 37000081004 | 4 BOTTLE, PLASTIC in 1 PACKAGE (37000-810-04) / 30 mL in 1 BOTTLE, PLASTIC |
| 37000-810-08 | 37000081008 | 236 mL in 1 BOTTLE, PLASTIC (37000-810-08) |
| 37000-810-12 | 37000081012 | 354 mL in 1 BOTTLE, PLASTIC (37000-810-12) |
| 37000-810-24 | 37000081024 | 2 BOTTLE, PLASTIC in 1 CELLO PACK (37000-810-24) / 236 mL in 1 BOTTLE, PLASTIC |
Linked data
RxNorm, label and prices
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 37000-810 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/37000-810 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 37000-810. 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.