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NDC 82711-103, Xylitol, Calcium Lactate, spray, from TOOTHFILM INC..

Product NDC
82711-103
Status
Listed
Labeler
TOOTHFILM INC.
Dosage form
SPRAY
Route
DENTAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82711-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CALCIUM LACTATE.02 mg/20mg
  • XYLITOL2 mg/20mg

Pharmacologic classes

Blood Coagulation Factor [EPC]; Calcium [CS]; Cations, Divalent [CS]; Increased Coagulation Factor Activity [PE]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]

Package NDCNDC-11Package
82711-103-02827110103021 BOTTLE in 1 BOX (82711-103-02) / 20 mg in 1 BOTTLE (82711-103-01)

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 82711-103 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82711-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82711-103. 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.