United States · FDA National Drug Code directory
Orajel Sensitivity Relief
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
- 10237-678_88d71cb7-8abf-407d-a74c-f5537497759a
- Product NDC
- 10237-678
- Form
- PASTE, DENTIFRICE
- Composition / generic term
- Sodium Fluoride and Potassium Nitrate
- Labeler
- Church & Dwight Co., Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20240131
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM FLUORIDE — .243 g/100g
- POTASSIUM NITRATE — 5 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TUBE in 1 CARTON (10237-678-12) / 170 g in 1 TUBE · 10237-678-12
- 121.9 g in 1 TUBE (10237-678-43) · 10237-678-43
Source and coverage
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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.
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