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WesTussin DM NF

NDC 69367-353, WesTussin DM NF, liquid, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-353
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
LIQUID
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M012
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-353 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENYLEPHRINE HYDROCHLORIDE7.5 mg/5mL
  • DEXTROMETHORPHAN HYDROBROMIDE15 mg/5mL
  • DEXBROMPHENIRAMINE MALEATE2 mg/5mL

Pharmacologic classes

Adrenergic alpha1-Agonists [MoA]; 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 NDCNDC-11Package
69367-353-1669367035316473 mL in 1 BOTTLE (69367-353-16)

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 69367-353 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-353 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-353. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.