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Tretinoin

NDC 68682-514, Tretinoin, gel, from Oceanside Pharmaceuticals.

Product NDC
68682-514
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA020475
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-514 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRETINOIN.4 mg/g

Pharmacologic classes

Retinoid [EPC]; Retinoids [CS]

Package NDCNDC-11Package
68682-514-92686820514921 TUBE in 1 CARTON (68682-514-92) / 20 g in 1 TUBE
68682-514-94686820514941 TUBE in 1 CARTON (68682-514-94) / 45 g in 1 TUBE
68682-514-95686820514951 BOTTLE, PUMP in 1 CARTON (68682-514-95) / 50 g in 1 BOTTLE, PUMP

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d3c528d2-429d-4f37-9ebf-eee8b9fd3050

Use it

Look up 68682-514 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-514 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-514. 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.