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PreviDent 5000 Dry Mouth

NDC 0126-0016, Sodium fluoride, gel, dentifrice, from Colgate Oral Pharmaceuticals, Inc..

Product NDC
0126-0016
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/0126-0016 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE6.1 mg/mL
Package NDCNDC-11Package
0126-0016-6100126001661100 mL in 1 BOTTLE (0126-0016-61)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d93ee76f-454b-40bf-9357-39a2ae3b6ccb

Use it

Look up 0126-0016 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0126-0016 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0126-0016. 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.