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NDC 59365-5030, Oxyquinoline Sulfate and Sodium Lauryl Sulfate, jelly, from CooperSurgical, Inc..

Product NDC
59365-5030
Status
Listed
Labeler
CooperSurgical, Inc.
Dosage form
JELLY
Route
VAGINAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59365-5030 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYQUINOLINE SULFATE.25 mg/g
  • SODIUM LAURYL SULFATE.1 mg/g
Package NDCNDC-11Package
59365-5030-059365503000113.4 g in 1 TUBE (59365-5030-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e4a1caa-e6ba-44ef-8347-07e6385a7c9e

  • NADAC price for package 59365503000

    GET /v1/drugs/nadac/59365503000

Use it

Look up 59365-5030 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59365-5030 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59365-5030. 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.