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First Aid Direct All Day Pain Relief

NDC 42961-122, Naproxen Sodium, tablet, coated, from Cintas Corporation.

Product NDC
42961-122
Status
Listed
Labeler
Cintas Corporation
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA204872
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42961-122 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN SODIUM220 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
42961-122-024296101220225 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01)

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 42961-122 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42961-122 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42961-122. 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.