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NDC 87846-001, SODIUM FLUORIDE, gel, dentifrice, from Dabur India Limited.

Product NDC
87846-001
Status
Listed
Labeler
Dabur India Limited
Dosage form
GEL, 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/87846-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE.24 g/100g
Package NDCNDC-11Package
87846-001-20878460001201 BOTTLE in 1 BOX (87846-001-20) / 113 g in 1 BOTTLE

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 87846-001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87846-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87846-001. 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.