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NDC 71614-002, ALLANTOIN, gel, from PARMA KOREA.

Product NDC
71614-002
Status
Listed
Labeler
PARMA KOREA
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71614-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALLANTOIN3 mg/mL
Package NDCNDC-11Package
71614-002-02716140002021 BOTTLE in 1 CARTON (71614-002-02) / 100 mL in 1 BOTTLE (71614-002-01)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

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

Use it

Look up 71614-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71614-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71614-002. 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.