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PureLife APF

NDC 68987-012, Sodium Fluoride, gel, from PureLife Dental.

Product NDC
68987-012
Status
Listed
Labeler
PureLife Dental
Dosage form
GEL
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/68987-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5.6 g/454g
Package NDCNDC-11Package
68987-012-1568987001215454 g in 1 BOTTLE, PLASTIC (68987-012-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/615840e4-c108-4d68-b815-fc95ae75539c

Use it

Look up 68987-012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68987-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68987-012. 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.