United States · FDA National Drug Code directory
Colgate Triple Action
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 35000-941_905181e2-96e2-4b14-9605-47353a251173
- Product NDC
- 35000-941
- Form
- PASTE, DENTIFRICE
- Composition / generic term
- SODIUM FLUORIDE
- Labeler
- Colgate-Palmolive Company
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20101201
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM FLUORIDE — 1.1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 3 TUBE in 1 CARTON (35000-941-30) / 170 g in 1 TUBE · 35000-941-30
- 1 TUBE in 1 CARTON (35000-941-48) / 226 g in 1 TUBE · 35000-941-48
- 1 TUBE in 1 CARTON (35000-941-58) / 70 g in 1 TUBE · 35000-941-58
- 1 TUBE in 1 CARTON (35000-941-60) / 170 g in 1 TUBE · 35000-941-60
- 1 TUBE in 1 CARTON (35000-941-69) / 113 g in 1 TUBE · 35000-941-69
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →