United States · FDA National Drug Code directory

DOCOSANOL

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
58602-019_6dcfa761-32bb-4b0e-b0c0-2bd44cfe99d9
Product NDC
58602-019
Form
CREAM
Composition / generic term
DOCOSANOL
Labeler
Aurohealth LLC
Marketing category
ANDA
Marketing start / end (source format)
20240301
Source listing expiry
20271231

Source-listed ingredients

  • DOCOSANOL — 100 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 PACKAGE (58602-019-08) / 2 g in 1 TUBE · 58602-019-08
  • 2 TUBE in 1 PACKAGE (58602-019-09) / 2 g in 1 TUBE · 58602-019-09
  • 1 TUBE in 1 PACKAGE (58602-019-11) / 3 g in 1 TUBE · 58602-019-11
  • 1 TUBE in 1 PACKAGE (58602-019-12) / 3 g in 1 TUBE · 58602-019-12
  • 2 TUBE in 1 PACKAGE (58602-019-13) / 3 g in 1 TUBE · 58602-019-13
  • 1 BOTTLE, PUMP in 1 PACKAGE (58602-019-15) / 2 g in 1 BOTTLE, PUMP · 58602-019-15
  • 1 BOTTLE, PUMP in 1 PACKAGE (58602-019-16) / 2 g in 1 BOTTLE, PUMP · 58602-019-16
  • 2 BOTTLE, PUMP in 1 PACKAGE (58602-019-17) / 2 g in 1 BOTTLE, PUMP · 58602-019-17
  • 1 TUBE in 1 PACKAGE (58602-019-24) / 2 g in 1 TUBE · 58602-019-24

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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