RoboHBr Cough SUPPRESSANT

Manufacturer
DXM Pharmaceutical, Inc
Effective date
2025-10-06
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:38:03

Label at a glance#

ProductRoboHBr Cough SUPPRESSANT
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE
Label structure8 sections

Indications and uses

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

Dosage and administration

only use this product according to these directions or as directed by a doctor do not exceed 4 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 1 tablet every 6 to 8 hours, as needed  children under 12 years  do not use Other Information store at 20-25°C (68-77°F). TAMPER EVIDENT: Do not use if safety s...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan Hbr 30 mg

Purpose

OTC - PURPOSE SECTION

Cough suppressant 

Uses

INDICATIONS & USAGE SECTION

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

Warnings

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.

Ask a doctor before use if you 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions 

DOSAGE & ADMINISTRATION SECTION

  • only use this product according to these directions or as directed by a doctor
  • do not exceed 4 tablets in any 24-hour period
  • this adult product is not intended for use in children under 12 years of age
AgeDose
 adults and children 12 years and over take 1 tablet every 6 to 8 hours, as needed
 children under 12 years do not use
  • Other Information
  • store at 20-25°C (68-77°F).
  • TAMPER EVIDENT: Do not use if safety seal under child-resistant cap is broken or missing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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.

Distributed by:
DXM Pharmaceutical, Inc. 2717 Commercial Center Blvd., Suite E200
Katy, TX 77 494
www.RoboCough.com Patent Pending.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2173856dextromethorphan hydrobromide 30 MG Oral TabletPSN9
2173856dextromethorphan hydrobromide 30 MG Oral TabletSCD9

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130371598100305GTIN-13: 0371598100305
EAN-13: 0371598100305
GTIN-12: 371598100305
UPC-A: 371598100305
GTIN storage (14 digits): 00371598100305
Image-1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71598-100-302023-09-20C16284748780-10191ceaa-7258-198a-e063-dbdaa90aec3eRoboTablets
71598-100-302023-09-20C16284748780-10191ceaa-7258-198a-e063-dbdaa90aec3eRoboTablets
71598-100-302023-07-28C16284748780-10191ceaa-7258-198a-e063-dbdaa90aec3eRoboTablets
71598-100-302023-07-28C16284748780-10191ceaa-7258-198a-e063-dbdaa90aec3eRoboTablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71598-100-30RoboHBr Cough SUPPRESSANT100 in 1 BOTTLE, PLASTICTABLET1009

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71598-10071598-100-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82023-10-17full-release2026-06-01 00:22:51

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
RoboHBr Cough SUPPRESSANTDEXTROMETHORPHAN HBRDXM Pharmaceutical, Inc0af624ce-191f-45e1-882b-e8acb90cc77b2025-10-06WarningsExact identifier
ndc (package): 71598-100-30
ndc (product): 71598-100
ndc11 (package): 71598010030
spl id: 4081add6-4a26-5ce8-e063-6394a90a8be7
spl set id: 0af624ce-191f-45e1-882b-e8acb90cc77b

Reported adverse events (FAERS/openFDA)#

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