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Foamgle Foam Super Mint

NDC 50555-220, Allantoin, mouthwash, from KMPHARMACEUTICAL CO.,LTD.

Product NDC
50555-220
Status
Listed
Labeler
KMPHARMACEUTICAL CO.,LTD
Dosage form
MOUTHWASH
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50555-220 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALLANTOIN.05 g/100mL
Package NDCNDC-11Package
50555-220-02505550220021 BOTTLE in 1 CARTON (50555-220-02) / 150 mL in 1 BOTTLE (50555-220-01)

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 50555-220 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50555-220 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50555-220. 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.