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Run: USP 795 Nonsterile Compounding Record and Beyond-Use Dating

Record each nonsterile compounding event, document ingredients and checks, and assign a beyond-use date using the USP 795 water-activity framework.

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Compounding Event Details

Record Date (required)

Compounding Date (required)

Compounding Time

Preparation Name (required)

Dosage Form (required)

Batch or Lot Reference

Internal batch identifier or compounding reference number for the audit trail.

Intended Use

Briefly describe the clinical or dispensing purpose. Collect only what is needed for the record.

Formula and Ingredients

Master Formula Reference (required)

Ingredients (required)

Equipment Used

Compounding Method (required)

Describe the method used, including any mixing, heating, levigation, or dilution steps.

Water Activity and Beyond-Use Date

Was Water Activity Measured? (required)

Water Activity Value (aw)

Enter the measured water activity value if available.

Water Activity Method

Assigned Beyond-Use Date (required)

BUD Assignment Basis (required)

BUD Rationale (required)

Explain how the beyond-use date was determined, including any water-activity result, formulation characteristics, and supporting references.

Quality Checks and Sign-Off

Final Inspection Completed (required)

Yes No N/A

Label Verified (required)

Yes No N/A

Deviations or Incidents

Document any deviations, errors, or corrective actions. Leave blank if none.

Preparer Name (required)

Reviewer Name

If your workflow requires review, record the reviewer here.

Signature (required)

Compliance and Disclosure

I understand this form collects limited personnel and compounding record information for quality, compliance, and audit trail purposes. (required)

Yes No N/A

What happens after I submit

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Email (required)

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