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AQUAFRESH CAVITY PROTECTION

NDC 0135-0590, sodium fluoride, paste, from Haleon US Holdings LLC.

Product NDC
0135-0590
Status
Listed
Labeler
Haleon US Holdings LLC
Dosage form
PASTE
Route
DENTAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M022
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0135-0590 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE1.15 mg/g
Package NDCNDC-11Package
0135-0590-01001350590011 TUBE in 1 CARTON (0135-0590-01) / 158.8 g in 1 TUBE
0135-0590-02001350590021 TUBE in 1 CARTON (0135-0590-02) / 85 g in 1 TUBE
0135-0590-04001350590042 TUBE in 1 CARTON (0135-0590-04) / 158.8 g in 1 TUBE
0135-0590-05001350590053 TUBE in 1 CARTON (0135-0590-05) / 158.8 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 0135-0590 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0135-0590 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0135-0590. 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.