Gels Durex Play

Product Safety and Regulatory Compliance – Durex Intimate Lubricants

Medical Device Classification

This product is a medical device intended to relieve vaginal dryness and improve comfort during intimate activity.

General Safety and Usage Information (GPSR)

• Instructions: Read the label and instructions carefully before use.
• Skin Reaction: For external use only. Avoid contact with eyes. If redness, burning or irritation occurs, discontinue use.
• Not a Contraceptive: This product is not a contraceptive and does not contain spermicidal ingredients.
• Fertility Notice: Some lubricants may slow sperm motility. If you are trying to conceive, consult a healthcare professional before use.
• Usage Limitations: Do not apply to damaged or irritated skin.
• After Opening: Use within 3 months after first opening.
• Storage: Store at room temperature in a cool, dry place. Protect from direct sunlight.
• Keep Out of Reach of Children.
• Package Integrity: Do not use if the packaging or seal is damaged.
• Compatibility: Suitable for use with condoms. Check product packaging for compatibility details.

Medical Device Certification

CE Marking – compliant with EU medical device regulations.

Notified Body: 1639 – SGS Belgium NV
Noorderlaan 87, 2030 Antwerp, Belgium.

Responsible Economic Operators

Manufacturer:
Reckitt Benckiser Healthcare (UK) Ltd
Dansom Lane, Hull, HU8 7DS, United Kingdom
Email: GRAMedicalDevices@reckitt.com

EU Authorized Representative:
RB NL Brands B.V.
Schiphol Blvd 207, 1118 BH Schiphol, Netherlands

Importer:
Reckitt Benckiser Deutschland GmbH
Darwinstraße 2–4, 69115 Heidelberg, Germany

EU Regulatory Reference:
Regulation (EU) 2023/988 of the European Parliament and of the Council of 10 May 2023 on general product safety.