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Colgate Triple Action

NDC 35000-941, SODIUM FLUORIDE, paste, dentifrice, from Colgate-Palmolive Company.

Product NDC
35000-941
Status
Listed
Labeler
Colgate-Palmolive Company
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M021
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/35000-941 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE1.1 mg/g
Package NDCNDC-11Package
35000-941-30350000941303 TUBE in 1 CARTON (35000-941-30) / 170 g in 1 TUBE
35000-941-48350000941481 TUBE in 1 CARTON (35000-941-48) / 226 g in 1 TUBE
35000-941-58350000941581 TUBE in 1 CARTON (35000-941-58) / 70 g in 1 TUBE
35000-941-60350000941601 TUBE in 1 CARTON (35000-941-60) / 170 g in 1 TUBE
35000-941-69350000941691 TUBE in 1 CARTON (35000-941-69) / 113 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 35000-941 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/35000-941 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 35000-941. 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.