MGC HEALTH- cough drops black cherry sugar free lozenge

MGC Health by

Drug Labeling and Warnings

MGC Health by is a Otc medication manufactured, distributed, or labeled by YUNNAN BAIYAO GROUP CO., LTD, Medical Group Care LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Menthol 5.8

Purpose

Purposes cough suppressant, oral anesthetic

Use

temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat

Warnings

Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or follow headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious.

ASK DOCTOR

Ask a doctor before use if you have: ■ persistent or chronic cough such as occurs with smoking, asthma, or emphysema ■ cough accompanied by excessive phlegm (mucus).

STOP USE

Stop use and ask a doctor if ■ cough persists for more than 1 week, tends to recur, or is accompained by fever, rash, or persistent headache. These could be signs of a serius condition. ■ sore mouth does not improve in 7 days ■ irritation, pain, or redness persists or worsens.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

adults and children 5 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed.

children under 5 years: ask a doctor.

Other information

phenylketonurics: contains phenylalanine 2 mg per drop

excessive consumption may have a laxative effect
contains: SOY.

-5 calories per drop

Inactive ingredients

Acesulfame potassium, aspartame, eucalyptus oil, maltitol, FD&C blue 1. FD&C red 40, flavors. isomalt, soy lecithin, sucralose, water.

QUESTIONS

Call Toll-Free 866-306-9136 or visit our website: www.mgc.us

customerservice@mgc.us

Package Label - Principal Display Panel

25 Drops NDC: 61658-127-25

INGREDIENTS AND APPEARANCE

MGC HEALTH 
cough drops black cherry sugar free lozenge

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61658-127
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5.8 mg

Inactive Ingredients
Ingredient Name	Strength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
EUCALYPTUS OIL (UNII: 2R04ONI662)
FD&C RED NO. 40 (UNII: WZB9127XOA)
ISOMALT (UNII: S870P55O2W)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
WATER (UNII: 059QF0KO0R)
ASPARTAME (UNII: Z0H242BBR1)

Product Characteristics
Color	red	Score	score with uneven pieces
Shape	OVAL	Size	21mm
Flavor	MENTHOL	Imprint Code	B
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61658-127-25	25 in 1 BAG; Type 0: Not a Combination Product	09/01/2023
2	NDC: 61658-127-70	70 in 1 BAG; Type 0: Not a Combination Product	09/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	09/01/2023

Labeler - YUNNAN BAIYAO GROUP CO., LTD (654223122)

Registrant - Medical Group Care LLC (085137089)