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PreviDent 5000 Sensitive

NDC 0126-0070, Sodium fluoride and Potassium nitrate, gel, dentifrice, from Colgate Oral Pharmaceuticals, Inc..

Product NDC
0126-0070
Status
Listed
Labeler
Colgate Oral Pharmaceuticals, Inc.
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/0126-0070 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE5.8 mg/mL
  • POTASSIUM NITRATE57.5 mg/mL
Package NDCNDC-11Package
0126-0070-6100126007061100 mL in 1 BOTTLE (0126-0070-61)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b028cfff-4946-49e8-b8bb-197ab99d0d35

Use it

Look up 0126-0070 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0126-0070 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0126-0070. 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.