Package Label.Principal Display Panel
NDC 70771-1873-2
Tretinoin cream USP, 0.1%
20 grams
Rx
Tretinoin Cream 20 G (650ffd6d E4dd 49df Be9e Da611704dc40 01)
Tretinoin Cream
FDA Label NDC 70771-1873
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zydus Lifesciences Limited for the product Tretinoin (NDC 70771-1873). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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