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Sensodyne Pronamel Clinical Enamel Strength Whitening Action

NDC 0135-0811, potassium nitrate, sodium fluoride, paste, from Haleon US Holdings LLC.

Product NDC
0135-0811
Status
Listed
Labeler
Haleon US Holdings LLC
Dosage form
PASTE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M022
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0135-0811 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM NITRATE50 mg/g
  • SODIUM FLUORIDE1.15 mg/g
Package NDCNDC-11Package
0135-0811-02001350811021 TUBE in 1 CARTON (0135-0811-02) / 96.4 g in 1 TUBE
0135-0811-03001350811031 TUBE in 1 CARTON (0135-0811-03) / 65.2 g in 1 TUBE
0135-0811-23001350811232 TUBE in 1 CARTON (0135-0811-23) / 96.4 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 0135-0811 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0135-0811 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0135-0811. 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.