Package Label.Principal Display Panel
NDC 70771-1981-1 in tube of 15 g
Mupirocin cream USP, 2%
Rx only
Tube Label (93a19ca4 Ca3b 4338 917f 8c0920628574 01)
Mupirocin Cream
FDA Label NDC 70771-1981
1 label section · Submitted to the FDA by Zydus Lifesciences Limited · 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 Mupirocin (NDC 70771-1981). 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.
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