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MICONAZOLE Nitrate 2%

NDC 71399-0071, MICONAZOLE NITRATE, cream, from Akron Pharma Inc..

Product NDC
71399-0071
Status
Listed
Labeler
Akron Pharma Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M005
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71399-0071 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MICONAZOLE NITRATE2 g/100g

Pharmacologic classes

Azole Antifungal [EPC]; Azoles [CS]

Package NDCNDC-11Package
71399-0071-1713990071011 TUBE in 1 BOX (71399-0071-1) / 14.2 g in 1 TUBE
71399-0071-3713990071031 TUBE in 1 BOX (71399-0071-3) / 28.4 g in 1 TUBE
71399-0071-4713990071041 TUBE in 1 BOX (71399-0071-4) / 42.5 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 71399-0071 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71399-0071 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71399-0071. 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.