United States · FDA National Drug Code directory
Zinc Oxide
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
- 67777-223_4f5b6507-0292-edc3-e063-6294a90a3c79
- Product NDC
- 67777-223
- Form
- OINTMENT
- Composition / generic term
- Zinc Oxide Ointment
- Labeler
- Dynarex Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20240229
- Source listing expiry
- 20271231
Source-listed ingredients
- ZINC OXIDE — 200 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 72 BOX in 1 CASE (67777-223-02) / 1 TUBE in 1 BOX (67777-223-11) / 28.4 g in 1 TUBE (67777-223-01) · 67777-223-02
- 72 BOX in 1 CASE (67777-223-04) / 1 TUBE in 1 BOX (67777-223-13) / 56.7 g in 1 TUBE (67777-223-03) · 67777-223-04
- 12 JAR in 1 CASE (67777-223-06) / 425 g in 1 JAR (67777-223-05) · 67777-223-06
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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