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SODIUM CHLORIDE HYPERTONICITY

NDC 73581-708, sodium chloride, ointment, from YYBA CORP.

Product NDC
73581-708
Status
Listed
Labeler
YYBA CORP
Dosage form
OINTMENT
Route
OPHTHALMIC
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M018
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73581-708 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE50 mg/mL

Pharmacologic classes

Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]

Package NDCNDC-11Package
73581-708-35735810708351 TUBE in 1 CARTON (73581-708-35) / 3.5 mL 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 73581-708 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73581-708 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73581-708. 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.