Betamethasone Dipropionate Ointment
FDA Label NDC 70771-1550

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 Betamethasone Dipropionate (NDC 70771-1550). 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

Package Label.Principal Display Panel

Betamethasone Dipropionate Ointment USP, 0.05%

NDC 70771-1550-1 in tube of 15 gm

Rx Only

Tube Label (3150c577 7edd 42c3 B0c7 Bae78fa2bb52 01)

Tube Label (3150c577 7edd 42c3 B0c7 Bae78fa2bb52 01)

Carton Label (3150c577 7edd 42c3 B0c7 Bae78fa2bb52 02)

Carton Label (3150c577 7edd 42c3 B0c7 Bae78fa2bb52 02)

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