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Sodium Sulfacetamide 8% and Sulfur 4%

NDC 71399-0487, SULFACETAMIDE SODIUM, SULFUR, suspension, from Akron Pharma Inc..

Product NDC
71399-0487
Status
Listed
Labeler
Akron Pharma Inc.
Dosage form
SUSPENSION
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/71399-0487 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFACETAMIDE SODIUM80 mg/mL
  • SULFUR40 mg/mL

Pharmacologic classes

Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]

Package NDCNDC-11Package
71399-0487-671399048706473 mL in 1 BOTTLE, PLASTIC (71399-0487-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bfbe625c-5679-4363-913a-2ab03198f4f0

Use it

Look up 71399-0487 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71399-0487 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71399-0487. 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.