Launching a food, health supplement, or wellness product in the UAE requires more than just a strong formulation and attractive packaging — it demands clear regulatory classification. Many businesses assume their product falls under Dubai Municipality (DM), only to face unexpected rejections, shipment holds, or penalties when it is deemed a MOHAP-regulated GSL product or medicine instead. Understanding when and why MOHAP regulation applies is critical for avoiding costly delays and ensuring a smooth market entry. This guide explains the key regulatory triggers, practical examples, and compliance steps to help you determine the correct authority for your product from the start.

Regulatory Overview

• Dubai Municipality (DM)
  • Oversees consumer products: food, beverages, health supplements
  • Focus: safety, labeling, composition
• Ministry of Health and Prevention (MOHAP)
  • Regulates General Sales List (GSL) products and medicines
  • Covers products intended to treat, prevent, or diagnose medical conditions
  • Includes products with active pharmaceutical ingredients (APIs) or therapeutic concentrations

Key Factors Triggering MOHAP Regulation

A.    Product Claims

• DM-appropriate claims:
  • General health/wellness (e.g., “supports immunity”)
  • Cosmetic/wellness benefits (e.g., “improves skin appearance”)
• MOHAP-triggering claims:
  • Disease-related (e.g., “reduces cholesterol,” “treats diabetes”)
  • Performance enhancement implying pharmacological effect (e.g., “boosts testosterone”)
  • Therapeutic or diagnostic implications

Tip: Avoid treatment, prevention, or diagnostic language if you wish to remain under DM.

B.     Ingredients

• Triggers for MOHAP regulation:
  • Pharmacologically active compounds
  • Herbal extracts with medicinal properties
  • Controlled substances or any medicine-classified ingredient

C.   Concentration / Dosage

• High doses may trigger MOHAP even if the ingredient is DM-approved
  • Vitamins/minerals above daily maximums
  • Botanical extracts with pharmacological effects
  • Amino acids or performance enhancers affecting metabolism or hormones

 Practical Examples

Steps to Ensure Proper Classification

1. Review product claims carefully
2. Evaluate ingredients and concentrations against DM and MOHAP limits
3. Consult regulatory experts if unsure
4. Document all rationale, calculations, and supporting references for inspections

How Bizzmosis Can Assist

• Regulatory Assessment: We review product claims, ingredients, and concentrations to determine the correct authority (DM or MOHAP) for registration.
• Registration Support: We prepare and submit registration dossiers to DM or MOHAP, ensuring compliance with local regulations.
• Documentation Guidance: We assist in compiling necessary lab reports, certificates, and labeling compliance documents.
• Follow-up & Liaison: We communicate with authorities on your behalf to expedite approval and handle queries efficiently.
• Post-Registration Advice: Guidance on renewals, variations, and ongoing compliance requirements.

Summary

• DM (Food/Health Supplement): General wellness claims + safe ingredient levels
• MOHAP (GSL Product/Medicine): Therapeutic claims, disease treatment/prevention implications, active pharmaceutical ingredients or pharmacological doses
• Proper classification is critical to avoid fines, delays, or market rejection

Need Help Classifying Your Product?

Incorrect classification between Dubai Municipality (DM) and MOHAP can result in rejected applications, shipment holds, fines, or costly rework.

At Bizzmosis, our regulatory specialists assess your product before submission, ensuring the correct authority, compliant claims, and accurate dosage limits from day one.

👉 Get a professional regulatory assessment today
📩 Email: hello@bizzmosis.com
📞 Call/WhatsApp: +971 52 979 8169