COLD AND FLU RELIEF- atropine, naja naja venom, magnesium chloride, potassium hydroxide spray 
PROTEGE' MEDIA LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active ingredient                                                                       Purpose

Contains atropine (Atropinum) 5X HPUS …………………………………....   runny nose relief
Contains cobra venom preparation (Naja naja) 5X HPUS ……….....  pain relief
Contains magnesium chloride (Magnesia muriatica) 5X HPUS…....  cold remedy
Contains potassium hydroxide (Kali causticum) 7X HPUS ………. .... flu remedy
Reference: the Homeopathic Pharmacopoeia of the United States (HPUS)

Contains 24 doses

Use

Temporarily relieves symptoms associated with colds and flu.

Warnings

If symptoms persist or worsen, discontinue use, seek medical attention.
• Avoid contact with eyes. If product gets into eyes, flush with water, seek medical attention.
• If pregnant or breastfeeding ask a health professional before use.
• Consult a medical professional if using other medications for known interactions.
• The use of this dispenser by more than one person may spread infection.

Keep out of reach of children.

Directions

Inactive ingredients

Aspartic acid, benzalkonium chloride, glycerin, propylene glycol, purified water, thiamine.

Comments, Questions or Complaints?

Call 888-735-4009 or info@promedxnow.com

Product label

image description

COLD AND FLU RELIEF 
atropine, naja naja venom, magnesium chloride, potassium hydroxide spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76524-501
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ATROPINE (UNII: 7C0697DR9I) (ATROPINE - UNII:7C0697DR9I) ATROPINE5 [hp_X]  in 0.2 mL
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM5 [hp_X]  in 0.2 mL
MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CATION5 [hp_X]  in 0.2 mL
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) (HYDROXIDE ION - UNII:9159UV381P) POTASSIUM HYDROXIDE7 [hp_X]  in 0.2 mL
Inactive Ingredients
Ingredient NameStrength
ASPARTIC ACID (UNII: 30KYC7MIAI)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
THIAMINE (UNII: X66NSO3N35)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76524-501-185 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/29/2020
Labeler - PROTEGE' MEDIA LLC (117063923)

Revised: 1/2021
Document Id: b8cf40a1-a3e2-3596-e053-2a95a90aa996
Set id: a434e7e2-31f6-4eee-864d-d4ef7c6b675d
Version: 1
Effective Time: 20210113
 
PROTEGE' MEDIA LLC