BUPROPIDEX- dextromethorphan hydrobromide tablet

BupropiDex by

Drug Labeling and Warnings

BupropiDex by is a Otc medication manufactured, distributed, or labeled by DXM Pharmacuetical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

(in each tablet) Dextromethrophan HBr 15 mg

Purpose

Cough suppressant

Uses

Temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold.

Warning

Do not useif 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 ifyou have
a cough that is accompanied by excessive phlegm (mucus), or
a persistent or chronic cough such as occurs with smoking, asthma, or emphysema.

Stop use and ask a doctor ifa cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

​Directions

• only use this product according to these directions or as directed by a doctor
• do not exceed 8 tablets in any 24-hour period.
• this adult product is not intended for use in children under 12 years of age.

• age: dose
• adults and children 12 years and over:

  take 2 tablets every 6 to 8 hours, as needed

• children under 12 years: do not use

Other information 

store at 20-25°C (68-77°F). Do not refrigerate.
TAMPER EVIDENT: Do not use if safety seal under child-resistant cap is broken or missing.

Inactive ingredients

magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

Call weekdays between 10 a.m. to 4 p.m. CST, at 833-289-7626 or visit our website www.RoboCough.com to report serious adverse events associated with the use of this product. Please call a doctor for medical advice.

SPL UNCLASSIFIED SECTION

Distributed by:
DXM Pharmaceutical, Inc. 2717 Commercial Center Blvd., Suite E200
Katy, TX 77 494

Copyright 2023. Patent Pending. www.RoboCough.com.

Product label

INGREDIENTS AND APPEARANCE

BUPROPIDEX 
dextromethorphan hydrobromide tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71598-200
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	DEX
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71598-200-15	200 in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	12/01/2023

Labeler - DXM Pharmacuetical, Inc. (080748277)

Registrant - DXM Pharmacuetical, Inc. (080748277)