Robitussin Day and Night Maximum Strength Cough DM
NDC 0031-2103, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, kit, from Haleon US Holdings LLC.
- Product NDC
- 0031-2103
- Status
- Listed
- Labeler
- Haleon US Holdings LLC
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M012
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0031-2103 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0031-2103-01 | 00031210301 | 1 KIT in 1 CARTON (0031-2103-01) * 1 BOTTLE in 1 CARTON (0031-8739-12) / 118 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0031-8718-13) / 118 mL in 1 BOTTLE |
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 0031-2103 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0031-2103 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0031-2103. 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.