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Oxymetazoline Hydrochloride

NDC 51672-1405, Oxymetazoline Hydrochloride, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1405
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213584
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1405 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYMETAZOLINE HYDROCHLORIDE10 mg/g

Pharmacologic classes

Imidazolines [CS]; Increased Sympathetic Activity [PE]; Vasoconstriction [PE]; Vasoconstrictor [EPC]

Package NDCNDC-11Package
51672-1405-2516721405021 TUBE in 1 CARTON (51672-1405-2) / 30 g in 1 TUBE
51672-1405-3516721405031 TUBE in 1 CARTON (51672-1405-3) / 60 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8a7f2400-5e18-4215-8d2c-f55881706107
  • NADAC price for package 51672140502

    GET /v1/drugs/nadac/51672140502

Use it

Look up 51672-1405 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1405 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1405. 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.