COUGH MEDICINE SOOTHING RELIEF- dextromethorphan liquid

COUGH MEDICINE by

Drug Labeling and Warnings

COUGH MEDICINE by is a Otc medication manufactured, distributed, or labeled by LM WHOLESALE HERBS, RFX Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each 10 ml)

Dextromethorphan Hydrobromide 30 mg

Purpose

Cough suppressant

Use

■ Temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold

Warnings

Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

■ cough that occurs with too much phlegm (mucus)

■ cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding

Keep out of reach of children

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

■ do not take more than 4 doses in any 24-hour period

■ one dose is one bottle

■ this adult product is not intended for use in children under 12 years of age

AgeDose

Adults and Children one bottle (10 ml)

12 years and over every 6-8 hours

Children under 12 years do not use

Inactive Ingredients

Apricot kernel oil, fritillaria delavayi bulb, honey, water

Other information

■ Store at 20C-25ºC (68F-77º F). Do not refrigerate

Questions or comments?

■ 1-800-860-0888

Package Label

INGREDIENTS AND APPEARANCE

COUGH MEDICINE  SOOTHING RELIEF
dextromethorphan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75663-002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	30 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
APRICOT KERNEL OIL (UNII: 54JB35T06A)
HONEY (UNII: Y9H1V576FH)
FRITILLARIA DELAVAYI BULB (UNII: AG6Q756AT7)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	brown (light brown)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75663-002-01	6 in 1 BOX	05/18/2020
1	NDC: 75663-002-10	10 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	05/18/2020

Labeler - LM WHOLESALE HERBS (104462911)

Establishment
Name	Address	ID/FEI	Business Operations
RFX Pharmaceutical Co., Ltd.		530620871	manufacture(75663-002)