Guaifenesin
NDC 60687-852, Guaifenesin, solution, from American Health Packaging.
- Product NDC
- 60687-852
- Status
- Listed
- Labeler
- American Health Packaging
- 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/60687-852 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GUAIFENESIN100 mg/5mL
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60687-852-17 | 60687085217 | 10 TRAY in 1 CASE (60687-852-17) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-852-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-852-40) |
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 60687-852 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-852 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-852. 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.