011013 Niacinamide 4% / Tretinoin 0.025%
FDA Label NDC 72934-2200

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sincerus Florida, Llc for the product 011013 Niacinamide 4% / Tretinoin 0.025% (NDC 72934-2200). 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 directions for use, adverse reactions, active, inactive, ndc 72934-2200-2 011013 niacinamide 4% / tretinoin 0.025% cream 30 gm, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Directions For Use

→ Adverse Reactions

→ Active, Inactive

→ Ndc 72934-2200-2 011013 Niacinamide 4% / Tretinoin 0.025% Cream 30 Gm

* Please review the disclaimer below.

Previous Product 72934-2179

Next Product 72934-2204