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NDC 52000-038, Menthol and Zinc Oxide, powder, from Universal Distribution Center LLC.

Product NDC
52000-038
Status
Listed
Labeler
Universal Distribution Center LLC
Dosage form
POWDER
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M016
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52000-038 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MENTHOL, UNSPECIFIED FORM1.5 mg/g
  • ZINC OXIDE10 mg/g

Pharmacologic classes

Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]

Package NDCNDC-11Package
52000-038-2552000003825283 g in 1 BOTTLE (52000-038-25)
52000-038-2652000003826226 g in 1 BOTTLE (52000-038-26)

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 52000-038 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52000-038 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52000-038. 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.