Robo Cough

Manufacturer
DXM Pharmacuetical, Inc. | DXM Pharmaceutical, Inc.
Effective date
2021-07-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:41:15

Label at a glance#

ProductRobo Cough
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE
Label structure13 sections

Storage and handling

Other information ​ ​store at 20-25* (68-77*F). Do not refigerate. TAMPER EVIDENT: Do not use if printed shrink band on bottle is broken or missing.

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

In each 3ml (one dose)

Dextromethrophan HBr 30 mg......................cough suppressant

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

​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.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • a cough that is accompanied by excessive phlegm (mucus), or
  • a persisten or chronic cough such as occurs with smoking, asthma, or emphysema.

OTC - STOP USE SECTION

Stop use and ask a doctor if​ a 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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

​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)

DOSAGE & ADMINISTRATION SECTION

​Directions

  • ​only use this product according to these directions or as directed by a doctor.
  • do not exceed 120 milligrams in any 24-hour period
  • measure only 3mL with dosing cup provided
  • keep dosing cup with product
  • mL= milliliter
  • this adult product is not intented for use in children under 12 years of age.
age dose
adults and children 12 years and over

3mL every 6 to 8 hours

children under 12 yearsdo not use

STORAGE AND HANDLING SECTION

Other information

  • ​​store at 20-25* (68-77*F). Do not refigerate.
  • TAMPER EVIDENT: Do not use if printed shrink band on bottle is broken or missing.

INACTIVE INGREDIENT SECTION

​Inactive ingredients​ high fructose corn syrup, methyl antrhaniliate (artificial grape flavor), phosphoric acid, propylene glycol, purified water, sodium benzoate (preservative), sucralose

OTC - QUESTIONS SECTION

​Questions or comments?

​Call 1-833-289-7626 between 10 a.m. to 4 p.m. CST, Monday through Friday 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.

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr........30mg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Distributed by:

DXM Pharmaceutical, Inc.

2717 Commercial Center Blvd.,

Suite E200

Katy, TX 77494

www.RoboCough.com

Patent Pending. Copyright 2018 DXM Pharmaceutical, Inc.

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71598-000-002023-12-13C16284748780-1e4f33bdf-9e2e-d8a0-e053-dadaa90a6e4eRobo Cough
71598-000-002022-07-29C16284748780-1e4f33bdf-9e2e-d8a0-e053-dadaa90a6e4eRobo Cough

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71598-00071598-000-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0c6426be-2152-9ac0-e063-6394a90ae09967ccc318-e73d-5b88-e053-2991aa0a0e4c2023-12-13WarningsExact identifier
spl set id: 67ccc318-e73d-5b88-e053-2991aa0a0e4c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.