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PureLife APF

NDC 68987-010, Sodium Fluoride, gel, from PureLife Dental.

Product NDC
68987-010
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/68987-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5.6 g/454g
Package NDCNDC-11Package
68987-010-1568987001015454 g in 1 BOTTLE, PLASTIC (68987-010-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/492a4a5b-a94d-4928-b0dd-976bb909c476

Use it

Look up 68987-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68987-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68987-010. 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.