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NDC 79481-5200, acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, doxylamine succinate, kit, from Meijer, Inc..
- Product NDC
- 79481-5200
- Status
- Listed
- Labeler
- Meijer, Inc.
- 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/79481-5200 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 79481-5200-0 | 79481520000 | 1 KIT in 1 CARTON (79481-5200-0) * 2 TABLET, FILM COATED in 1 BLISTER PACK (41250-569-00) * 2 TABLET, FILM COATED in 1 BLISTER PACK (79481-0099-0) |
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 79481-5200 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/79481-5200 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 79481-5200. 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.