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Orajel Sensitivity Relief

NDC 10237-678, Sodium Fluoride and Potassium Nitrate, paste, dentifrice, from Church & Dwight Co., Inc..

Product NDC
10237-678
Status
Listed
Labeler
Church & Dwight Co., Inc.
Dosage form
PASTE, DENTIFRICE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M021
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10237-678 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE.243 g/100g
  • POTASSIUM NITRATE5 g/100g
Package NDCNDC-11Package
10237-678-12102370678122 TUBE in 1 CARTON (10237-678-12) / 170 g in 1 TUBE
10237-678-4310237067843121.9 g in 1 TUBE (10237-678-43)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

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

Use it

Look up 10237-678 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10237-678 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10237-678. 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.