Water-based Personal Lubricant, Acvioo 001
FDA Label NDC 71847-2215

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Dikailong Technology Ltd for the product Water-based Personal Lubricant, Acvioo 001 (NDC 71847-2215). 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 active ingredient, inactive ingredient, purpose, when using, do not use, stop use, ask doctor, ask doctor/pharmacist, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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