Delivers a precise, consistent dose of fine mist for intranasal application, supporting saline rinses, decongestants, allergy relief sprays, and other nasal care formulations. Engineered for dosing accuracy and repeatability, with actuator designs available to meet pharmaceutical and consumer healthcare requirements.
Nasal spray pumps are engineered for precise, low-volume dosing rather than broad-area misting, and are available in a range of actuator styles, dose volumes, and safety features to suit different formulations. Buyers can choose from standard, metered-dose, and child-resistant/tamper-evident options, along with pharmaceutical-grade material certifications to meet regulatory requirements. Dip tube lengths are fully customizable, ensuring a precise fit with the bottle of your choice.
Standard actuator, metered-dose (calibrated), child-resistant, unit-dose, bidirectional spray
0.05ml – 0.14ml per actuation
18mm, 20mm crimp, 13mm, 15mm snap-on
APR-certified, 100% recyclable PP/PE options available
Electroplating, color spray, metal wrap, hot stamping, silkscreen printing.
Find quick answers to common questionsabout our products, services, and capabilities.
Nasal spray pumps are engineered for precise intranasal dosing, delivering much smaller volumes than cosmetic mist pumps (typically 0.05–0.14ml per actuation, versus 1ml+ for facial mists), and require tighter control over spray cone angle and droplet distribution to ensure effective deposition on the nasal mucosa. Before selecting a supplier, clarify whether the product is positioned as pharmaceutical/OTC or cosmetic/personal care, since precision and compliance requirements differ significantly between the two.
If the product label states a specific active ingredient dose per spray (e.g., antihistamine or decongestant sprays), a metered-dose pump is required to ensure consistent output volume across actuations (typically within ±10% tolerance). For non-drug applications like saline rinses, a standard actuator is usually sufficient and more cost-effective.
Common reference standards include ISO 20072 (testing for nasal sprays, pumps, and dropper dispensers) and USP <1601> (performance testing for nasal sprays and inhalers). If the product will be sold as an OTC drug or medical device in the US or EU, also confirm the supplier’s GMP manufacturing status and relevant registration documentation — request certification proof during the RFQ stage.
Nasal spray pumps commonly use 18mm crimp fittings or 13mm/15mm snap-on fittings, which differ from standard cosmetic bottle necks (e.g., 18-410, 20-410 threaded finishes). Coordinate with your bottle supplier early to confirm fitting type, neck inner diameter, and crimp height to avoid leakage or sealing failures.
For products containing active drug ingredients (e.g., medicated nasal sprays) sold in consumer markets, most regions require child-resistant or tamper-evident packaging to comply with safety regulations (such as the US PPPA). Confirm the specific regulatory requirements for your target market before sourcing, and request corresponding certification from your supplier.
Standard, non-metered nasal spray pumps usually have an MOQ around 50,000–100,000 units. Metered-dose pumps or products requiring GMP-certified production lines often carry higher MOQs (100,000+ units) and longer lead times due to additional dose calibration and batch testing. Custom actuator designs, child-resistant mechanisms, or specific certification requirements can extend lead times further — plan to start sourcing 3–6 months ahead of your target launch.
Request spray pattern test reports and droplet size distribution data from your supplier, and consider third-party lab verification against ISO 20072 standards where needed. These metrics directly affect drug deposition and delivery efficacy in the nasal cavity — critical for pharmaceutical-grade product acceptance and not something that can be assessed by appearance or feel alone.
Internal pump components (springs, gaskets, mesh filters) must be compatible with the formulation to avoid material leaching, discoloration, or seal failure. Before scaling production, conduct extractables & leachables testing and accelerated stability testing, and request a material compliance declaration from your supplier (e.g., PFAS-free, BPA-free) to ensure long-term safety.
Tell us a bit about your information, and our team will reach out as soon as possible.
