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NDC 40171-005, polyethylene glycol 400, solution/ drops, from Bausch & Lomb Incorporated.

Product NDC
40171-005
Status
Listed
Labeler
Bausch & Lomb Incorporated
Dosage form
SOLUTION/ DROPS
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/40171-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POLYETHYLENE GLYCOL 4002.5 mg/mL
Package NDCNDC-11Package
40171-005-05401710005055 VIAL, SINGLE-USE in 1 CARTON (40171-005-05) / .4 mL in 1 VIAL, SINGLE-USE
40171-005-254017100052525 VIAL, SINGLE-USE in 1 CARTON (40171-005-25) / .4 mL in 1 VIAL, SINGLE-USE
40171-005-3640171000536180 VIAL, SINGLE-USE in 1 CARTON (40171-005-36) / .4 mL in 1 VIAL, SINGLE-USE

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 40171-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/40171-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 40171-005. 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.