GILTUSS HONEY DM COUGH- dextromethorphan hbr solution

Giltuss Honey DM Cough by

Drug Labeling and Warnings

Giltuss Honey DM Cough by is a Otc medication manufactured, distributed, or labeled by Dextrum Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Active Ingredients ( in each 10 ml)

Dextromethorphan, 30 mg

Purpose and uses

Purpose

Cough supresant

Uses

Temporary relieves:

Cough due to minor throat and bronchial irritation associated with the common cold or inhaled irritants, the intensity of coughing ,the impulse to cough to help you get sleep,

Warning

Warnings

Do not use

If you are taking a prescription monoamine oxidase inhibitor (MAOI) ( certains drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you dont know is your prescription drug contains and MAOI, ask a doctor or pharmacist before taking this product.

Ask a Doctor

Ask a doctor before use if you have, a cough with too much phlegm (mucus) , a persistent or chronic cough as occurs with smoking, asthma, chronic bronchitis, or emphysema.

Stop use

Stop use and ask a doctor if

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

If Pregnant

If pregnant or breast- feeding, ask a health professional before use. Keep out of reach of children.

In case of accidental overdose, get medical or professional help or contact a Poisson Control center immediately

Indication and usage section

Do not take more than 4 doses in any 24 hours period

Use enclosed dosing cup

Keep dosing cup for use with this product

ml= mililiters

Adults and children 12 years & over 10 ml every 6-8 hours

children 6 to under 12 years of age 5 ml every 6-8 hours

children 4 to under 6 years of age 2.5 ml every 6-8 hours

children under 4 years of age Consult a doctor

Other information

Other information

Store at room temperature 15-30 °C (59° -86 ° F)
Close cap tightly
SAVE CARTON FOR COMPLETE DRUG FACTS

Inactive ingredients

Inactive ingredients

natural and artificial flavor, natural grade A honey, methylparaben, potassium sorbate, propylene glycol, propylparaben, purified water, sucralose

Dosage

Dosage and administration

Do not take more than 4 doses in any 24 hours period

Use enclosed dosing cup

Keep dosing cup for use with this product

ml= mililiters

Adults and children 12 years & over 10 ml every 6-8 hours

children 6 to under 12 years of age 5 ml every 6-8 hours

children 4 to under 6 years of age 2.5 ml every 6-8

Keeo out of the reach of children.

Keeo out of the reach of children.

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

Principal panel

Maximum strength

Alcohol free, dye free, Non-Drowsy

The source Cerified Honey

Giltus Honey DM

Cough

Dextromethorphan HBr, 30 mg

Persistent Cough

Up to 8 hours

Honey lemon flavor

4 floz 118 ml

INGREDIENTS AND APPEARANCE

GILTUSS HONEY DM COUGH 
dextromethorphan hbr solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65852-004
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
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
HONEY (UNII: Y9H1V576FH)
METHYLPARABEN (UNII: A2I8C7HI9T)
SUCRALOSE (UNII: 96K6UQ3ZD4)
WATER (UNII: 059QF0KO0R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Product Characteristics
Color		Score
Shape		Size
Flavor	HONEY (Lemon)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65852-004-04	1 in 1 CARTON	06/22/2020
1		118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	06/22/2020

Labeler - Dextrum Laboratories, Inc (007392322)