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AquaSoothe

NDC 67777-555, AquaSoothe, ointment, from Dynarex Corporation.

Product NDC
67777-555
Status
Listed
Labeler
Dynarex Corporation
Dosage form
OINTMENT
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M016
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67777-555 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PETROLATUM41 g/100g
Package NDCNDC-11Package
67777-555-026777705550224 TUBE in 1 CASE (67777-555-02) / 106 g in 1 TUBE (67777-555-01)
67777-555-046777705550412 JAR in 1 CASE (67777-555-04) / 396.9 g in 1 JAR (67777-555-03)
67777-555-066777705550612 BOX in 1 CASE (67777-555-06) / 144 PACKET in 1 BOX (67777-555-05) / .9 g in 1 PACKET

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 67777-555 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67777-555 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67777-555. 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.