FDA Label for Mydcombi

1 Indications And Usage

MYDCOMBI (tropicamide and phenylephrine hydrochloride ophthalmic spray) 1% / 2.5% is indicated to induce mydriasis for diagnostic procedures and in conditions where short term pupil dilation is desired.

2.1 Recommended Dosage

Administer one metered spray to the cornea of each eye to be dilated. Repeat after 5 minutes.

Other

Pediatric Patients Younger Than 1 Year Old

In pediatric patients younger than 1 year old, administer one metered spray to the cornea of each eye to be dilated, up to a maximum of 3 sprays per eye per day.

Risk Summary

There are no available data on MYDCOMBI use in pregnant women or animals to inform any drug-associated risks. It is also not known whether tropicamide or phenylephrine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. MYDCOMBI should be given to a pregnant woman only if clearly needed.

Risk Summary

There are no data on the presence of tropicamide or phenylephrine in human milk from the administration of MYDCOMBI, the effects on the breastfed infant, or the effects on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for MYDCOMBI and any potential adverse effects on the breastfed child from MYDCOMBI.

Manufactured for Eyenovia, Inc. by Alcami Corporation

2.2 Administration Instructions

The following steps should be followed sequentially:

• Load the MYDCOMBI dispenser by depressing the FILL BUTTON at the top of the dispenser once.

  Figure 1 - mydcombi 01

  Figure 1: MYDCOMBI Dispenser Front (L) and Back (R) View
• Hold MydCombi™ dispenser with thumb over Mist Button, wrapping other fingers around base.
• Bring MydCombi™ dispenser to patient's eye with Mirror facing the eye.
  • –The dispenser should be as close as patient's nose.
  • –To prevent blinking, use your other hand to gently pull lower eyelid down or ask patient to pull her/his lid down.
  • Aim Mist Opening toward the center of eye.
  • Confirm Alignment Marks (on the Fill Button and the cartridge side) align with the center of eye.
    • –Ask patient to confirm when their eye is centered on the BLUE Mirror.
    If patient is having trouble centering their eye on the blue light, ask that they look up, then look at the BLUE Mirror.
    • Firmly press and release Mist Button.
      • –The drug solution should gently wet the eye. Repeat steps A to F if needed.
      • Administer a second metered spray after 5 minutes to each dilated eye.
      • Repeat steps A to G for the contralateral eye if it is to be dilated.
      
      

3 Dosage Forms And Strengths

MYDCOMBI is a sterile, clear, colorless, topical ophthalmic spray containing tropicamide 1% (w/w) and phenylephrine hydrochloride 2.5% (w/w). Each metered spray delivers 0.008 mL which contains 0.08 mg tropicamide and 0.2 mg phenylephrine hydrochloride.

4.1 Known Hypersensitivity

Contraindicated in persons showing known hypersensitivity to any component of the formulation.

5.1 Topical Ophthalmic Use

MYDCOMBI is not indicated for injection.

5.2 Blood Pressure Elevation

Caution should be exercised with the use of MYDCOMBI in pediatric patients less than 5 years of age and patients with hyperthyroidism, or cardiovascular disease. The post-treatment blood pressure of patients with cardiac and endocrine diseases and any patients who develop symptoms should be carefully monitored.

5.3 Central Nervous System Disturbances

Tropicamide in MYDCOMBI may cause CNS disturbances which may be dangerous in pediatric patients. The possibility of psychotic reactions and behavioral disturbances due to hypersensitivity to anticholinergic drugs should be considered.

5.4 Intraocular Pressure

Mydriatics may produce a transient elevation of intraocular pressure.

5.5 Rebound Miosis

Rebound miosis has been reported one day after receiving phenylephrine hydrochloride ophthalmic solution, and re-administration of the drug produced a lesser mydriatic effect.

6 Adverse Reactions

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The most common adverse reactions (incidence < 2%) were transient blurred vision, reduced visual acuity, photophobia, and mild eye discomfort.

6.1 Ocular Adverse Reactions

Transient blurred vision, reduced visual acuity, photophobia, superficial punctate keratitis, and mild eye discomfort may occur. Increased intraocular pressure has been reported following the use of mydriatics.

6.2 Systemic Adverse Reactions

Dryness of the mouth, tachycardia, headache, allergic reactions, nausea, vomiting, pallor, central nervous system disturbances and muscle rigidity have been reported with the use of tropicamide. Psychotic reactions, behavioral disturbances, and vasomotor or cardiorespiratory collapse in children have been reported with the use of anticholinergic drugs.

A marked increase in blood pressure has been reported with the use of phenylephrine, particularly, but not limited to, low weight premature neonates, infants, and hypertensive patients.

7.1 Agents That May Exaggerate Pressor Responses

Phenylephrine in MYDCOMBI may enhance the pressor effects of atropine-like drugs and induce tachycardia in some patients.

7.2 Cholinergic Agonists And Ophthalmic Cholinesterase Inhibitors

Tropicamide in MYDCOMBI may interfere with the antihypertensive action of carbachol, pilocarpine, or ophthalmic cholinesterase inhibitors.

7.3 Potent Inhalation Anesthetic Agents

Phenylephrine in MYDCOMBI may potentiate the cardiovascular depressant effects of some inhalation anesthetic agents.

8.4 Pediatric Use

Tropicamide in MYDCOMBI may rarely cause CNS disturbances which may be dangerous in pediatric patients. Psychotic reactions, behavioral disturbances, and vasomotor or cardiorespiratory collapse in children have been reported with the use of anticholinergic drugs [see Warnings and Precautions (5.3)].

8.5 Geriatric Use

No overall differences in safety or effectiveness of MYDCOMBI have been observed between patients 65 years of age and older and younger adult patients.

10 Overdosage

Overdosage of MYDCOMBI may cause a rapid rise in blood pressure. It may also cause headache, anxiety, nausea and vomiting, and ventricular arrhythmias. Prompt injection of a rapidly acting alpha- adrenergic blocking agent such as phentolamine has been recommended.

11 Description

MYDCOMBI is a sterile, clear, colorless fixed dose combination of an anticholinergic (tropicamide) and an alpha-adrenergic receptor agonist (phenylephrine hydrochloride) for topical ophthalmic use. The 2 active ingredients are represented by the chemical structures below.

Tropicamide:

Chemical Structure - mydcombi 02

Chemical Name: Benzeneacetamide, N-ethyl-α-(hydroxymethyl)-N-(4-pyridinylmethyl)-

Molecular Formula: C₁₇H₂₀N₂O₂

Molecular Weight: 284.35 g/mol

Phenylephrine Hydrochloride:

Chemical Name: (R)-3-hydroxy-α[(methylamino)methyl]benzenemethanol hydrochloride

Molecular Formula: C₉H₁₃NO₂∙HCl

Molecular Weight: 203.67 g/mol

Each mL of MYDCOMBI ophthalmic spray (sterile) contains: ACTIVES: Phenylephrine Hydrochloride 2.5% (25 mg) equivalent to 20.6 mg of phenylephrine base, Tropicamide 1% (10 mg); INACTIVE: Hydrochloric Acid and/or Sodium Hydroxide may be added to adjust pH (pH 4.8–5.2), Water for Injection; PRESERVATIVE: Benzalkonium Chloride 0.01% (0.1 mg).

12.1 Mechanism Of Action

Tropicamide, the anticholinergic component of MYDCOMBI, blocks the responses of the sphincter muscle of the iris, dilating the pupil (mydriasis). Phenylephrine hydrochloride, the alpha-1 adrenergic agonist component of MYDCOMBI, acts as a mydriatic agent by contracting the dilator muscle of the iris.

12.2 Pharmacodynamics

MYDCOMBI acts in 15 to 30 minutes with maximal mydriasis occurring in 20 to 90 minutes. Darker irides tend to dilate slower than lightly pigmented irides and to achieve maximal effect may require more doses than lighter irides.

Mydriasis will reverse spontaneously with time, with recovery after 3 to 8 hours. Complete recovery from mydriasis in some individuals may require 24 hours.

13 Clinical Studies

Two Phase 3 clinical trials were conducted to evaluate the efficacy of MYDCOMBI for achievement of mydriasis. The MIST-1 study was a prospective, double-masked, active-controlled, 3-period cross-over, superiority study to compare the pupil dilating effect of MYDCOMBI to tropicamide 1% and to phenylephrine 2.5%, with all solutions topically administered by the Optejet^® Dispenser (N = 64 subjects; 128 eyes). The MIST-2 study was a prospective, multicenter, double-masked, placebo-controlled, 3-period crossover, superiority study to compare the pupil dilating effect of MYDCOMBI to placebo (eyewash solution), with both solutions topically administered by the Optejet Dispenser (N = 70 subjects; 140 eyes).

The primary efficacy endpoint for both studies was the mean change in 35-minute pupil diameter compared to baseline as measured by digital pupillometry in highly photopic conditions. Data from the 2 studies are presented in Table 1. At 35 minutes post-dose, the mean change in pupil diameter was 4.7 mm with MYDCOMBI, 4.1 mm with tropicamide, and 0.9 mm with phenylephrine in MIST-1, and was 4.8 mm with MYDCOMBI and 0.1 mm with placebo in MIST-2. MYDCOMBI was statistically superior to tropicamide administered alone and phenylephrine administered alone.

MYDCOMBI provided a clinically significant effect in the proportion of eyes achieving pupil diameter of ≥ 6 mm at 35-minute post-dose in 94% of eyes compared to 78% of eyes administered tropicamide alone and 1.6% of eyes administered phenylephrine alone, and 0% of eyes administered placebo. As shown in Figure 2, peak effect was measured at the 80-minute evaluation when the mean change from baseline was 5.2 mm. Treatment differences in mydriasis were observed as early as 20 minutes and still present at 180 minutes post-dose, the end of the protocol-specified observation period.

Figure 2 - mydcombi 04

Figure 2: MIST-1 and MIST-2 pooled, mean pupil diameter vs measurement time, by treatment group. Vertical bars show 95% confidence interval for the mean at each point. Smooth curves are based on an 8 degrees of freedom (df) generalized additive model (GAM) smooth through time, adjusting for baseline pupil diameter. Confidence intervals are not adjusted for correlation.

14 How Supplied/Storage And Handling

MYDCOMBI is supplied as sterile, clear, colorless solution in a 2 mL vial enclosed in a dispenser cartridge. Each MYDCOMBI cartridge holds approximately 180 sprays.

Do not tamper with or attempt to open the MYDCOMBI cartridge. Such action may damage the dispenser causing an incorrect medication discharge volume; additionally, the dispenser base may not function properly.

Only use the MYDCOMBI cartridge with the MYDCOMBI Dispenser base which may be supplied separately. The MYDCOMBI base will not work with any other cartridges.

NDC 81046-0111-1. Carton containing one replacement sterile drug cartridge

NDC 81046-0111-2. Box containing one carton with one sterile drug cartridge, and one carton with one base unit

NDC 81046-0111-5. Box containing five cartons, each with one replacement sterile drug cartridge

The MYDCOMBI cartridge must be used prior to the expiration date on the cartridge.

Storage And Handling

Storage: Store at room temperature 15°C to 25°C (59°F to 77°F).

15 Patient Counseling Information

Advise patients that they may experience sensitivity to light and blurred vision while their pupils are dilated.

Advise patients not to drive, use machinery, or do any activity that requires clear vision until they are sure they can perform such activities safely.

Instructions For Use

MydCombi™
(Tropicamide and Phenylephrine HCl Ophthalmic Spray), 1%/2.5%

Rx Only

INSTRUCTIONS FOR USE
MydCombi™ Ophthalmic Spray

This "Instructions for Use" document has information about the administration of MydCombi™ (Tropicamide and Phenylephrine HCI Ophthalmic Spray) 1%/2.5%.

MydCombi™ is packaged in a dispenser that mists drug solution onto the eye. It has 2 parts – the cartridge that holds the drug solution, and the base that holds electronics.

Getting to know MydCombi™

MydCombi™ Dispenser Parts	MydCombi™ Assembled
Figure - mydcombi 05

How the MydCombi™ Dispenser Works

• The MydCombi™ Cartridge holds the drug solution.
• The MydCombi™ Base supplies power to the dispenser.
• The Fill Button is pressed to load the drug solution for topical ophthalmic administration.
• The Mist Opening is where drug solution comes out when the Mist Button is pressed.
• The Light and Mirror around the Mist Opening and the Eye Alignment Marks on the top and each side of the cartridge help align the eye for drug administration.
• The Battery Light shows how much electrical charge remains in the Base.
• The Release Tabs on each side of the cartridge are used to separate the cartridge and base when replacing cartridges.
• The MydCombi™ Base is charged using a Micro-USB to USB Cable with Wall Plug or USB port (supplied separately). See "MydCombi™ Base Charging and Electrical Information" .

Understanding the Mist and Battery Lights

The Mist Light and the Battery Light show the status of the MydCombi™ dispenser.

See "TROUBLESHOOTING TIPS" (page 10) for dispenser reset instructions. If lights continue blinking after dispenser reset, reset again. If lights continue to blink after second reset, change the cartridge.

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	What the Mist and Battery Lights Mean
	If you see…	It means…
	Mist Light SOLID BLUE	Ready to dose
	Mist Light BLINKING BLUE with Battery Light BLINKING RED & BLUE	Reset the dispenser
	Battery Light BLINKING GREEN	Battery is charging
	Battery Light SOLID GREEN	Battery is fully charged
	Battery Light BLINKING RED	Battery is low
	Battery Light SOLID RED	Charge dispenser base at once

Important Reminders and Cleaning Instructions

• Wash hands prior to using MydCombi™.
• Before each use, the exterior (including the mirror surface) of the dispenser should be cleaned using a 70% isopropyl alcohol (IPA) wipe or a clean dust-free, cotton cloth dampened with 70% IPA solution.
• Wipe the exterior for 3 minutes. While wiping, pay close attention to all cracks, crevices, and any other hard to reach areas. Additional wipes may be used as needed. Allow the exterior to air dry. Only manual, non-immersion cleaning as described should be used for the dispenser. Do not autoclave (steam sterilize) or immerse in cleaning fluids. Always disconnect power supply from source before cleaning.
• If the patient wears soft contact lenses, they should be removed at least 10 minutes before drug administration.
• If the patient uses artificial tears, they should not be administered within 10 minutes of drug administration.
• Each MydCombi™ cartridge holds approximately 180 sprays.
• Only use the MydCombi™ cartridge with the MydCombi™ base. The MydCombi™ base will not work with any other type of cartridges.
• See "MydCombi™ Base Charging and Electrical Information" contained with MydCombi™ for complete instruction on charging and applicable electrical information.

Storing the MydCombi™ Base and Cartridges

Store MydCombi™ bases and cartridges at room temperature 15°C to 25°C (59°F to 77°F). Protect from light and excessive heat.

• -Do not heat or freeze the MydCombi™ base or cartridge.
• -Do not expose MydCombi™ base to fluids.
• -Do not tamper with or try to open the MydCombi™ cartridge or base. Doing so could cause damage and result in personal injury.

The MydCombi™ base contains a lithium-ion battery. Damage to the base can cause fire. Do not puncture base or expose to excessive heat (≥ 50°C).

Li-Ion batteries may pose environmental and safety hazards and should be disposed of in accordance with all applicable Federal and State Laws. Check with all governing travel bodies for current requirements before air travel.

Assembling the MydCombi™ Dispenser

Complete these steps to assemble the MydCombi™ base and cartridge.

Note: If packaging is opened or damaged, do not use the contents. Instead, open a new base or cartridge, and contact your distributer for a replacement.

Assemble
Remove base and/or cartridge from packaging.
Align base and cartridge, then press together until they click.
Take care to avoid pressing Fill Button when assembling.Charge
Charge MydCombi™ base before first use (see "MydCombi Base Charging and Electrical Information" contained with MydCombi™ base packaging). Charging may be performed either before or after assembly.
Push micro-USB cable into Charging Port.
Connect opposite end of USB cable to wall outlet plug or USB port.
Battery light BLINKS GREEN while charging.
Charge until battery light turns SOLID GREEN, then disconnect cable from Charging Port.Note: Excessive charging may damage battery or decrease battery life. Charging weekly, or when the Battery Light begins blinking red (signaling low battery) is recommended. Prime
Hold MydCombi™ dispenser upright.
Firmly press Fill Button down until it stops, and Mist Light turns Blue.
Slowly release Fill Button, while counting to 3.
If Fill Button does not return to position, press again until it is all the way down.
If Fill Button still does not return to position, get a new cartridge, and re-assemble (Steps 1 - 2 [page 6]).
Point Mist Opening away from face.
Firmly press, then release Mist Button.
Repeat Steps a – e until mist emerges from opening.
If mist does not come out after repeating these steps 5 times, get a new cartridge and re-assemble (Steps 1 - 2 [page 6]).
MydCombi™ is now ready to use.

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4.

Preparing MydCombi™ for Use Each Day

Load drug solution
Hold MydCombi™ dispenser upright.
Firmly press Fill Button down until it stops, and Mist Light turns Blue.
Slowly release Fill Button, while counting to 3.
If Fill Button does not return to position, press again until it is all the way down.
If Fill Button still does not return to position, get a new cartridge, and re-assemble (Steps 1 - 2 [page 6]). Do a test mist
Holding MydCombi™ dispenser upright, point Mist Opening away from face.
Firmly press and release Mist Button.
MydCombi™ is ready to use.

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Important: A test mist must be performed each day before dosing is commenced.

Administering MydCombi™

Load drug solution
Hold MydCombi™ dispenser upright and firmly press Fill Button down until it stops, and Mist Light turns Blue.
Slowly release Fill Button, while counting to 3.Align MydCombi™ with patient's eye
Hold MydCombi™ dispenser with thumb over Mist Button, wrapping other fingers around base.
Bring MydCombi™ dispenser to patient's eye with Mirror facing the eye.
The dispenser should be as close as patient's nose.
To prevent blinking, use your other hand to gently pull lower eyelid down or ask patient to pull her/his lid down.
Aim Mist Opening toward the center of eye.
Confirm Alignment Marks (on the Fill Button and the cartridge side) align with the center of eye.
Ask patient to confirm when their eye is centered on the BLUE Mirror.If patient is having trouble centering their eye on the blue light, ask that they look up, then look at the BLUE Mirror.Press Mist Button
Firmly press and release Mist Button.
The drug solution should gently wet the eye. Repeat Steps 1-3 if needed.

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Important: Keep MydCombi™ dispenser upright during use to maintain dose volume.

Troubleshooting Tips

• If no mist comes out when Mist Button is pressed, confirm Fill Button has been pressed down completely, and has returned to the "up" position.
• If solution is not administered within 1 minute after loading, it will be automatically discharged - the MIST Light will blink blue while the Battery Light blinks red and blue. The MydCombi™ dispenser must be reset using the steps below.
  To reset dispenser:
  • -Press and release Mist Button.
  • -Press and release Fill Button.
  • -Press and release Mist Button again.
  • -Reload solution (Step 1 [page 9]).

  To report suspected adverse reactions please contact Eyenovia, Inc at 1-833-393-6684 (Option 1) or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch.

  Replacing the MydCombi™ Cartridge

  Remove cartridge
  Hold MydCombi™ base in one hand. With other hand, press and squeeze Release Tabs on each side of cartridge.
  Pull cartridge and base apart.
  Place used cartridge in original tray and box for disposal or recycling.

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  Symbols Used in Labels on the MydCombi™ Cartridge, Base and Packaging

  SYMBOL	DEFINITION		SYMBOL	DEFINITION
  	CAUTION, CONSULT ACCOMPANYING DOCUMENTS			USE BY (YYYY-MM: YEAR-MONTH)
  	SEE INSTRUCTIONS FOR USE			STERILIZED USING ETHYLENE OXIDE
  	CATALOG NUMBER			NON-STERILE
  	BATCH CODE			DO NOT RESTERILIZE
  	QUANTITY			LITHIUM-ION BATTERY - TO BE APPROPRIATELY RECYCLED
  	DATE OF MANUFACTURE (YYYY-MM : YEAR-MONTH)			KEEP DRY
  	MANUFACTURER			GHS LITHIUM-ION DISPOSAL
  	DO NOT USE IF THE PACKAGING HAS BEEN OPENED OR DAMAGED			ELECTRONIC EQUIPMENT. DO NOT THROW IN TRASH.
  	WARNING: ELECTRICITY			BY PRESCRIPTION ONLY
  	PROTECTED AGAINST VERTICALLY FALLING WATER DROPS UP TO 15-DEGREE ANGLE			TYPE BF PART COMPLYING WITH IEC 60601-1

  Manufactured By:
  Eyenovia
  295 Madison Ave., Suite 2400
  New York, NY 10017

  © 2022 Eyenovia, Inc. All rights reserved.

  
  

Mydcombi™ Base Charging And Electrical Information

Figure - mydcombi 38

1. Charging the Mydcombi™ Base

NOTE: Do not use base if packaging is opened or damaged. Get a new package by contacting your Eyenovia sales representative or calling 1-833-393-6684 (choose Option 1).

2. Specifications for Mydcombi Base and Charger

3. EMC

This device has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in professional medical equipment. This equipment generates, uses, and radiates radio frequency energy and, if not prepared and used in accordance with instructions, may cause harmful interference to radio communications. There is no guarantee, however, that interference will not occur in a particular setting. If this device does cause harmful interference to radio or television reception, which can be determined by turning the device off/on, the user is encouraged to try to correct the interference by one or more of the following measures:

• Reorient or relocate the receiving antenna
• Increase the separation between the device and receiver
• Connect the device into an outlet on a circuit different from that to which the receiver is connected
• Consult the dealer or an experienced radio/TV technician for help

Note: Changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the device.

Guidance and Manufacturer's Declaration

This device is intended for use in the electromagnetic environment specified below. The device user should assure use in such an environment.

Electromagnetic emissions
Emissions Test		Compliance
RF emissions CISPR 11		Group 1
RF emissions CISPR 11		Class B
Harmonic Emissions IEC 61000-3-2		Class B
Voltage Fluctuations/Flicker emissions IEC 61000-3-3		Complies
Electromagnetic immunity
Phenomena of a continuous nature		Shall operate as intended. Shall be no degradation of performance. Shall be no loss of function.
Phenomena of transient nature		Functions shall be self-recoverable. Shall operate as intended after recovering. Shall be no degradation of performance,
Power interruption exceeding a certain time		Functions shall be recoverable by the operator. Shall operate as intended after recovering. Shall be no degradation of performance.
Immunity Test	IEC 60601 Test Level		Compliance Level
Electrostatic fast transient/burst IEC 61000-4-4 (Charging Only)	±2 kV for power supply lines		±2 kV for power supply lines
Surge IEC 61000-4-5 EN/IEC 61000-4-3 L-N (Charging Only)	±1 kV differential mode		±1 kV differential mode
EN/IEC 61000-4-3 (Charging Only)	Radiated Immunity 3 V/m, 80 – 2700 MHz 80% AM at 1 kHz & Proximity Fields from RF Wireless Communications Equipment		Radiated Immunity 3 V/m, 80 – 2700 MHz 80% AM at 1 kHz & Proximity Fields from RF Wireless Communications Equipment
Voltage dips, short interruptions, and voltage variations on power supply input lines IEC 61000-4-11	Voltage Dips 30% reduction, 25/30 periods At 0°		Voltage Dips 30% reduction, 25/30 periods At 0°
	Voltage Dips > 95% reduction, 0.5 period At 0°, 45°, 90°, 135°, 180°, 225°, 270°, and 315°		Voltage Dips > 95% reduction, 0.5 period At 0°, 45°, 90°, 135°, 180°, 225°, 270°, and 315°
	Voltage Dips > 95 reduction, 1 period At 0°		Voltage Dips > 95 reduction, 1 period At 0°
	Voltage Interruptions > 95% reduction, 250/300 periods		Voltage Interruptions > 95% reduction, 250/300 periods
Conducted RF EN/IEC 61000-4-6	Continuous Conducted RF, 80% AM (1 kHz) 3 Vrms, 0.15-80 MHz 6 Vrms in ISM and amateur radio Bands within 150kHz – 80MHz		Continuous Conducted RF, 80% AM (1 kHz) 3 Vrms, 0.15-80 MHz 6 Vrms in ISM and amateur radio Bands within 150kHz – 80MHz
Magnetic field IEC 61000-4-8	Power Frequency Magnetic Field 30Arms/m at 50/60Hz		Power Frequency Magnetic Field 30Arms/m at 50/60Hz

Immunity to RF Wireless Communications Equipment
Test Frequency (MHz)	Band For some services, only uplink frequencies are included. (MHz)	Service	Modulation The carrier shall be modulated using a 50% duty cycle square wave signal.	Max. Power (W)	Distance (m)	Immunity test level (V/m)
385	380 –390	TETRA 400	Pulse 18 Hz	1.8	0.3	27
450	430 – 470	GMRS 460, FRS 460	FM As an alternative to FM modulation, 50% pulse modulation at 18 Hz may be used because, while it does not represent actual modulation, it would be worst case. ± 5 kHz Deviation 1 kHz sine	2	0.3	28
710	704 – 787	LTE Band 13, 17	Pulse 217 Hz	0.2	0.3	9
745
780
810	800 – 960	GSM 800/900, TETRA 800, iDEN 820, CDMA 850, LTE Band 5	Pulse 18 Hz	2	0.3	28
870
930
1720	1 700 – 1 990	GSM 1800; CDMA 1900; GSM 1900; DECT; LTE Band 1, 3, 4, 25; UMTS	Pulse 217 Hz	2	0.3	28
1845
1970
2450	2 400 – 2 570	Bluetooth, WLAN, 802.11 b/g/n, RFID 2450, LTE Band 7	Pulse 217 Hz	2	0.3	28
5240	5 100 – 5 800	WLAN 802.11 a/n	Pulse 217 Hz	0.2	0.3	9
5500
5785

Recommended separation distances between portable and mobile RF communications equipment and the device, except for the distances indicated in the following table "Immunity to RF Wireless Communications Equipment".
The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. Users can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the device as recommended below, according to the maximum output power of the communications equipment.
Rated maximum output power of transmitter (W)	Separation distance according to frequency of transmitter (m)
	150 kHz to 80 MHz d = 1.2√P	80 MHz to 800 MHz d = 1.2√P	800 MHz to 2.7 GHz d = 2.3√P
0.01	0.12	0.12	0.23
0.1	0.38	0.38	0.73
1	1.2	1.2	2.3
10	3.8	3.8	7.3
100	12	12	23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

4. Disposal

• Contains Lithium-Ion Battery
  Lithium-Ion batteries may pose environmental and safety hazards and should be disposed of in accordance with all applicable Federal and State laws.
• Electronic Equipment
  Base should be properly disposed of in accordance with all applicable State and Federal laws.

5. Notes on Safety

Warnings and Recommendations

• Contains Lithium-Ion Battery
  Damage can cause fire. Do not puncture. Do not expose to excessive heat (≥ 50°C).
• Do not use after expiration date
  Expiration date is published on base label. Discontinue use if expiration date has passed.
• Inspect for device damage
  Do not use if package has been opened or damaged or if there is evidence of base damage. Doing so could result in injury.
• Tampering with parts in the Mydcombi™ Base
  Do not tamper with or attempt to open the base. Doing so could cause damage and result in personal injury.
• Risk of usage
  Failure to use base in accordance with instructions could affect dose dispensation. Keep base in upright position during use. If base has been idling for an extended period, dispense a waste spray. Optejet will not dispense drug while the base is actively charging.
• Risk due to insufficient user training
  Use base only with Mydcombi™ Cartridge. Refer to "Instructions for Use - Mydcombi™ Ophthalmic Spray".
• Risk due to battery leakage
  Do not use base if there is any sign of battery leakage.
• Keep dry
  Do not expose base to fluids; keep dry.
• Transportation and Storage
  Do not store or transport base with sharp or metallic objects.
• Risk of electrical leakage
  Non-hazardous voltage is present during normal use.
• Do not use with other equipment
  
• Do not use with non-certified USB charger
  Recharge base using a micro-USB cable (not included). Use of a charger other than that specified in Section 2 - Specifications could result in increased electromagnetic emissions or decreased electromagnetic immunity of the base, resulting in improper operation.
  CAUTION – For professional use
  Federal law restricts this device to sale by or on the order of a physician (21 CFR§801.109(b)(1)).
  CAUTION – Radiation emission
  This device emits electromagnetic radiation.

6. Reporting to Manufacturer and Authorities

If a serious incident occurs in connection with this device that affects the user or another person, please report incident to Eyenovia by calling 1-833-393-6684 (choose Option 1) or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch.

7. Symbols Used in Labels on Mydcombi™ Base and Packaging

SYMBOL	DEFINITION		SYMBOL	DEFINITION
	CAUTION, CONSULT ACCOMPANYING DOCUMENTS			USE BY (YYYY-MM: YEAR-MONTH)
	SEE INSTRUCTIONS FOR USE			ELECTRONIC EQUIPMENT. DO NOT THROW IN TRASH.
	CATALOG NUMBER			NON-STERILE
	BATCH CODE			KEEP DRY
	QUANTITY			LITHIUM-ION BATTERY - TO BE APPROPRIATELY RECYCLED
	DATE OF MANUFACTURE (YYYY-MM : YEAR-MONTH)			MANUFACTURER
	WARNING: ELECTRICITY			CAUTION: FEDERAL LAW RESTRICTS THIS PRODUCT
	PROTECTED AGAINST VERTICALLY FALLING WATER DROPS UP TO 15-DEGREE ANGLE			TYPE BF PART COMPLYING WITH IEC 60601-1

MANUFACTURED BY	Contact / Return Goods Policy
Eyenovia, Inc. 8748 Technology Way, Reno, NV 89521 © 2022 Eyenovia, Inc. All rights reserved. www.eyenovia.com	Contact your sales representative or Eyenovia for product returns. Call 1-833-EYENOVIA (393-6684) [email protected]

Principal Display Panel - Mydcombi Base Unit Label

MydCombi™ Base
Non-Sterile

REF FG-16427
LOT F-#####
YYYY-MM-DD

Li-ion

15°C
59°F

25°C
77°F

IPX2

Eyenovia, Inc.
295 Madison Ave, Ste 2400
New York, NY 10017

(01) 008600099909700
(10) F-123465
(17) 250405

Rx ONLY
LS-17076-E

Principal Display Panel - MYDCOMBI Base Unit Label - mydcombi 57

Principal Display Panel - Mydcombi Base Unit Carton

eyenovia

Rx ONLY
LS-17075-D

REF FG-16427 MydCombi™ Base
LOT F-#####
QTY 1

USE BY YYYY-MM-DD

YYYY-MM-DD

Eyenovia, Inc.
295 Madison Ave, Ste 2400
New York, NY 10017

Li-ion

NON
STERILE

IPX2

15°C
59°F

25°C
77°F

Principal Display Panel - MYDCOMBI Base Unit Carton - mydcombi 58

Principal Display Panel - Mydcombi Base Single Carton Label

LS-17078-D

MydCombi_™

Tropicamide and Phenylephrine
HCl Ophthalmic Spray 1% / 2.5 %

For Topical Ophthalmic Use

Exp: YYYY-MM
LOT ############

Manufactured for:
Eyenovia, Inc.
295 Madison Ave, Ste 2400
New York, NY 10017

NDC 81046-0111-1

Sterile 1.9mL Rx Only

Principal Display Panel - MYDCOMBI Base Single Carton Label - mydcombi 59

Principal Display Panel - Mydcombi Base Single Carton

MydCombi_™

Sterile

Rx Only

Tropicamide and Phenylephrine HCl
Ophthalmic Spray 1% / 2.5 %

MydCombi Cartridge
NDC 81046-0111-1

LOT ##########
QTY 1

YYYY-MM

Eyenovia, Inc.
295 Madison Ave, Ste 2400
New York, NY 10017

STORAGE
Store at room temperature 15°C to 25°C (59°F to 77°F).

Principal Display Panel - MYDCOMBI Base Single Carton - mydcombi 60

Principal Display Panel - Mydcombi Cartridge And Base Carton

Rx ONLY
LS-17081-D

MydCombi_™

NDC: 81046-0111-2

Tropicamide and Phenylephrine HCl Ophthalmic Spray 1% / 2.5 %

MydCombi Cartridge

STORAGE
Store at room temperature 15°C to 25°C (59°F to 77°F).
QTY 1

BASE UNIT

REF FG-16427 MydCombi Base
QTY 1

STORAGE
Store at room temperature 15°C to 25°C (59°F to 77°F).

Eyenovia, Inc.
295 Madison Avenue, Suite 2400
New York, NY 10017

Li-ion

NON
STERILE

IPX2

15°C
59°F

25°C
77°F

Principal Display Panel - MYDCOMBI Cartridge and Base Carton - mydcombi 61

Principal Display Panel - Mydcombi Cartridge And Base 5 Pack Box

MydCombi_™

QTY 5

Sterile
Rx Only

Tropicamide and
Phenylephrine HCl
Ophthalmic Spray 1% / 2.5 %

Eyenovia, Inc.
295 Madison Avenue, Suite 2400
New York, NY 10017

MydCombi Cartridge
NDC 81046-0111-5

STORAGE
Store at room temperature 15°C to 25°C (59°F to 77°F).

NDC: 81046-0111-05
SN: ABC098DEF765GHI432JK
EXP: YYYY-MM
Lot: MCL123

LOT ##########

YYYY-MM

LS-17079-E

Principal Display Panel - MYDCOMBI Cartridge and Base 5 Pack Box - mydcombi 62