United States · FDA National Drug Code directory

Obagi Nu-Derm System Normal-Dry Skin Transformation Trial

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: 62032-913_f1292c32-db82-4875-b681-b984c56f9cff
Product NDC: 62032-913
Form: KIT
Composition / generic term: HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE
Labeler: Obagi Cosmeceuticals LLC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start / end (source format): 20191202
Source listing expiry: 20261231

Source-listed ingredients

Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.

These values do not establish equivalence or a dose recommendation.

Packages

Package details are not available in this snapshot.

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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