COLD AND FLU RELIEF- allium cepa, antimon tart, arnica, baptisia, eupatorium perf, gelsemium, kali bic, lachesis, mer iod rub, sticta , sulphur iod, urtica ur liquid

Cold and Flu Relief by

Drug Labeling and Warnings

Cold and Flu Relief by is a Homeopathic medication manufactured, distributed, or labeled by Eight and Company L.L.C, King Bio Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients: Allium cepa 30C, Antimon tart 200C, Arnica 4X, Baptisia 4X, Eupatorium perf 200C, Gelsemium 200C, Kali bic 200C, Lachesis 200C, Merc iod rub 200C, Sticta 200C, Sulphur iod 200C, Urtica ur 200C.

WARNINGS

Warnings: ​If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INDICATIONS & USAGE

Temporarily relieves the common symptoms of cold and flu, including:

• sinus congestion
• achiness
• chills
• headache and fever

-Natural

-Gluten & Lactose free

-No artificial flavors or colors

-Vegetarian

-No known negative side effects

-No known negative drug interactions

DOSAGE & ADMINISTRATION

• Adults and children over 12: 2 sprays into the mouth each 30 minutes as needed for symptom relief the first day, 2 sprays 3 times a day thereafter.
• Children under 12: consult a health care professional.

OTHER SAFETY INFORMATION

Other Information: Do not use if the transparent seal around spray bottle is broken or missing.

INACTIVE INGREDIENT

Inactive Ingredients: Non-GMO glycerin, v/v, organic alcohol 20% v/v, purified water.

PURPOSE

Temporarily relieves the common symptoms of cold and flu, including:

• sinus congestion
• achiness
• chills
• headache and fever

-natural

-gluten & lactose free

-no artifical flavors or colors

-vegetarian

-no known negative side effects

-no known negative drug interactions

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

COLD AND FLU RELIEF 
allium cepa, antimon tart, arnica, baptisia, eupatorium perf, gelsemium, kali bic, lachesis, mer iod rub, sticta , sulphur iod, urtica ur liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61096-1002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	30 [hp_C]  in 41 mL
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5)	ANTIMONY POTASSIUM TARTRATE	200 [hp_C]  in 41 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	4 [hp_X]  in 41 mL
BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU)	BAPTISIA TINCTORIA ROOT	4 [hp_X]  in 41 mL
EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E)	EUPATORIUM PERFOLIATUM FLOWERING TOP	200 [hp_C]  in 41 mL
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q)	GELSEMIUM SEMPERVIRENS ROOT	200 [hp_C]  in 41 mL
POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V)	POTASSIUM DICHROMATE	200 [hp_C]  in 41 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	200 [hp_C]  in 41 mL
MERCURIC IODIDE (UNII: R03O05RB0P) (MERCURIC IODIDE - UNII:R03O05RB0P)	MERCURIC IODIDE	200 [hp_C]  in 41 mL
LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T)	LOBARIA PULMONARIA	200 [hp_C]  in 41 mL
SULFUR IODIDE (UNII: L6L8KA2AA0) (SULFUR IODIDE - UNII:L6L8KA2AA0)	SULFUR IODIDE	200 [hp_C]  in 41 mL
URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9)	URTICA URENS	200 [hp_C]  in 41 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61096-1002-1	1 in 1 CARTON	02/19/2019
1		41 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/19/2019

Labeler - Eight and Company L.L.C (927364120)

Registrant - Eight and Company L.L.C (927364120)