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Safe-Rx LLC

US

Last updated May 31, 2026

What Safe-Rx LLC makes

Safe-Rx LLC produces child-resistant medicine bottles and corresponding bottle caps designed to prevent accidental ingestion by young children. These products are intended for use with oral medications to enhance safety in household settings.

The company’s portfolio is regulated under the FDA’s Unique Device Identification (UDI) system in the United States. These devices fall under the classification of over-the-counter drug packaging and are subject to compliance with FDA labeling and safety standards.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Safe-Rx LLC manufacture?

Safe-Rx LLC specializes in child-resistant medicine bottles and their corresponding bottle caps. These devices are designed to reduce the risk of accidental medication ingestion by young children, ensuring safer storage of oral medications in homes. The focus is on enhancing safety for over-the-counter and prescription drugs.

Where is Safe-Rx LLC based, and how does that affect its regulatory oversight?

Safe-Rx LLC is based in the United States, which means its devices are subject to FDA regulations. Since these products fall under over-the-counter drug packaging, they must comply with U.S. labeling and safety standards, including the FDA’s Unique Device Identification (UDI) system for tracking and traceability.

Are Safe-Rx LLC’s devices listed in any regulatory registries, and why does this matter?

Yes, Safe-Rx LLC’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures transparency and traceability of medical devices in the U.S., helping healthcare providers, regulators, and patients verify product authenticity, recall status, and compliance with safety requirements.

How are Safe-Rx LLC’s devices classified under medical device regulations?

Safe-Rx LLC’s child-resistant medicine bottles and caps are classified as over-the-counter drug packaging under FDA guidelines. This classification means they must meet specific safety and labeling standards to ensure proper use, particularly in preventing child access to medications, while still allowing easy administration by caregivers.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
080632475

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Safe Rx 18 dram cap and ring blue 50 pack
FDA UDI
N/AActive
Safe Rx 60 dram cap and ring blue 50 pack
FDA UDI
N/AActive

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