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PRO Gel 5000 Mint

NDC 61578-215, Sodium fluoride, gel, dentifrice, from DENTAL ALLIANCE HOLDINGS LLC.

Product NDC
61578-215
Status
Listed
Labeler
DENTAL ALLIANCE HOLDINGS LLC
Dosage form
GEL, DENTIFRICE
Route
DENTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/61578-215 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5000 ug/g
Package NDCNDC-11Package
61578-215-016157802150168 g in 1 TUBE, WITH APPLICATOR (61578-215-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f127e236-5207-948b-e053-2a95a90ab740

Use it

Look up 61578-215 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/61578-215 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 61578-215. 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.