MDFARMA COLD AND FLU RELIEF- atropine, naja naja venom, magnesium chloride, potassium hydroxide spray

MDFARMA COLD and FLU RELIEF by

Drug Labeling and Warnings

MDFARMA COLD and FLU RELIEF by is a Otc medication manufactured, distributed, or labeled by Green Earth Health Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

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

PURPOSE

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

Keep out of reach of children.

Directions

• Do not use if tamperproof cover is missing.
• Press down 2-3 times to prime the pump.
• Spray once into each nostril
• Use 2 times per day to relieve discomfort.

Inactive ingredients

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

Comments, Questions or Complaints?

In the U.S. call 833-604-7128, 9:00am - 5:00pm Eastern Standard Time, Monday - Friday, except U.S. holidays or visit www.mdfarma.com available 24 hours.

Product label

INGREDIENTS AND APPEARANCE

MDFARMA COLD AND FLU RELIEF 
atropine, naja naja venom, magnesium chloride, potassium hydroxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73002-713
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATROPINE (UNII: 7C0697DR9I) (ATROPINE - UNII:7C0697DR9I)	ATROPINE	5 [hp_X]  in 0.2 mL
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM)	NAJA NAJA VENOM	5 [hp_X]  in 0.2 mL
MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM CATION	5 [hp_X]  in 0.2 mL
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) (HYDROXIDE ION - UNII:9159UV381P)	POTASSIUM HYDROXIDE	7 [hp_X]  in 0.2 mL

Inactive Ingredients
Ingredient Name	Strength
ASPARTIC ACID (UNII: 30KYC7MIAI)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
THIAMINE (UNII: X66NSO3N35)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73002-713-03	5 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/23/2020

Labeler - Green Earth Health Inc. (116983264)

Registrant - Green Earth Health Inc. (116983264)