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Sodium Sulfacetamide 9% - Sulfur 4%

NDC 71399-0482, SULFACETAMIDE SODIUM, SULFUR, suspension, from Akron Pharma Inc..

Product NDC
71399-0482
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/71399-0482 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFACETAMIDE SODIUM90 mg/mL
  • SULFUR40 mg/mL

Pharmacologic classes

Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]

Package NDCNDC-11Package
71399-0482-671399048206473 mL in 1 BOTTLE, PLASTIC (71399-0482-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/173fd4d6-1efb-46e3-bf8e-565a265b6d6e

Use it

Look up 71399-0482 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71399-0482 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71399-0482. 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.