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SODIUM SULFACETAMIDE AND SULFUR

NDC 44523-748, Sodium Sulfacetamide 9.8% and Sulfur 4.8%, emulsion, from BioComp Pharma, Inc..

Product NDC
44523-748
Status
Listed
Labeler
BioComp Pharma, Inc.
Dosage form
EMULSION
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/44523-748 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFACETAMIDE SODIUM98 mg/g
  • SULFUR48 mg/g

Pharmacologic classes

Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]

Package NDCNDC-11Package
44523-748-1044523074810285 g in 1 BOTTLE, PLASTIC (44523-748-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1ba8bb47-6f7a-28ec-e063-6394a90a8eb3

Use it

Look up 44523-748 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/44523-748 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 44523-748. 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.