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NDC 37000-995, Sodium Fluoride and Potassium Nitrate, paste, dentifrice, from The Procter & Gamble Manufacturing Company.

Product NDC
37000-995
Status
Listed
Labeler
The Procter & Gamble Manufacturing 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/37000-995 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM NITRATE50 mg/g
  • SODIUM FLUORIDE1.4 mg/g
Package NDCNDC-11Package
37000-995-52370000995521 TUBE in 1 CARTON (37000-995-52) / 147 g in 1 TUBE
37000-995-70370000995701 TUBE in 1 CARTON (37000-995-70) / 198 g in 1 TUBE

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 37000-995 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/37000-995 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 37000-995. 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.