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Theraflu Severe Cold Relief Daytime Berry Burst

NDC 0067-6800, Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride, powder, from Haleon US Holdings LLC.

Product NDC
0067-6800
Status
Listed
Labeler
Haleon US Holdings LLC
Dosage form
POWDER
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/0067-6800 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE20 mg/1
  • PHENYLEPHRINE HYDROCHLORIDE10 mg/1

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
0067-6800-02000676800026 POWDER in 1 CARTON (0067-6800-02)

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 0067-6800 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0067-6800 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0067-6800. 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.