Pentrexcilina Children TOTAL RELIEF Multi-Symptom

Manufacturer
OPMX LLC
Effective date
2026-09-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-30 01:01:14

Label at a glance#

ProductPentrexcilina Children TOTAL RELIEF Multi-Symptom
Active ingredientPHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Label structure16 sections

Indications and uses

temporarily relieves these common cold and flu symptoms: sinus congestion and pressure minor aches and pains nasal congestion cough due to minor throat and bronchial irritation sore throat headache temporarily reduces fever temporarily promtoes nasal and/or sinus drainage helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Dosage and administration

do not take more than directed (see Overdose warning) do not take more than 6 doses in any 24 hour period measure only with dosing cup provided do not use dosing cup with other products dose as follows or as directed by a doctor mL=mililiter tsp=teaspoonful Age Dose Children 6 to under 12 years of age 10 mL or 2 tsp provided every 4 hours Children under 6 years of age do not use

Storage and handling

each 10 mL contains: sodium 10mg store between 20-25°C (68-77°F) do not refrigerate keep carton for complete Drug Facts

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

in each 10mL 2 teaspoonful

Acetaminophen 250mg

Dextromethorphan HBr 13.33mg

Guaifenesin USP 200mg

Phenylephrine HCl 5 mg

Purpose

OTC - PURPOSE SECTION

Pain reliever/fever reducer

Cough suppressant

Expectorant

Nasal descongestant

Uses

INDICATIONS & USAGE SECTION

temporarily relieves these common cold and flu symptoms:

  • sinus congestion and pressure
  • minor aches and pains
  • nasal congestion
  • cough due to minor throat and bronchial irritation
  • sore throat
  • headache
  • temporarily reduces fever
  • temporarily promtoes nasal and/or sinus drainage
  • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Warnings

SPL UNCLASSIFIED SECTION

Liver warning

WARNINGS SECTION

This product contains acetaminophen.

Severe liver damage may occur if you take:

  • more than 6 doses in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product

Allergy alert

WARNINGS SECTION

Acetaminophen may cause severe skin reactions. Symptoms may include:

  • skin reddening
  • blisters
  • rash

If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning

WARNINGS SECTION

If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use

OTC - DO NOT USE SECTION

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
  • for children under 12 years of age
  • 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

OTC - ASK DOCTOR SECTION

  • liver disease
  • heart disease
  • diabetes
  • thyroid disease
  • high blood pressure
  • trouble urinating due to an enlarged prostate gland
  • persistent or chronic cough such as occurs with smoking, asthma chronic bronchitis, or emphysema
  • cough that occurs with too much phlegm (mucus)

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • taking the blood thinning drug warfarin
  • taking sodium restricted diet

When using this product

OTC - WHEN USING SECTION

do not exceed recommended dose (see overdose warning).

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • nervousness, dizziness, or sleeplessness occur
  • pain, nasal congestion, or cough gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • cough comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Overdose warning

OVERDOSAGE SECTION

Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical even if you do not notice any sings or symptms.

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not take more than directed (see Overdose warning)
  • do not take more than 6 doses in any 24 hour period
  • measure only with dosing cup provided
  • do not use dosing cup with other products
  • dose as follows or as directed by a doctor
  • mL=mililiter
  • tsp=teaspoonful
AgeDose
Children 6 to under 12 years of age10 mL or 2 tsp provided every 4 hours
Children under 6 years of agedo not use

Other information

STORAGE AND HANDLING SECTION

  • each 10 mL contains:
  • sodium 10mg
  • store between 20-25°C (68-77°F)
  • do not refrigerate
  • keep carton for complete Drug Facts

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe vera, citric acid, disodium EDTA, FD&C red no. 40, hydroxyethyl cellulose, natural & artificial strawberry flavor, propylene glycol USP, purified water, sodium benzoate, sorbitol 70% USP, sucralose.

Questions?

OTC - QUESTIONS SECTION

Call 619-600-5632 MN to FRI, 9 a.m. to 6 p.m. PTZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAXIMUM STRENGHT

NDC 69729-789-06

PENTREXCILINA

TOTAL RELIEF

ACETAMINOPHEN

DEXTROMETORPHAN HBr

PHENYLEPHRINE HCl

GUAIFENESIN

CHILDREN

Flu

Cold &

Cough

  • FEVER
  • BODYACHE
  • HEADACHE
  • SORE THROAT

6fl oz (177ml)

VERSIÓN EN ESPAÑOL EN EL INTERIOR DE LA CAJA

Exclusively distributed by:

OPMX

Chula Vista, CA 91910

Manufactured in FDA Registered in the USA

P4FLOZCHILDRENP4FLOZCHILDREN

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810053181539GTIN-13: 0810053181539
EAN-13: 0810053181539
GTIN-12: 810053181539
UPC-A: 810053181539
GTIN storage (14 digits): 00810053181539
_Pentrexcilina 4fl oz CHILDREN TOTAL_2_001.jpg
QR code linkQR Codeopmx.us/_Pentrexcilina 4fl oz CHILDREN TOTAL_2_001.jpg

DailyMed Product Concepts#

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Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69729-78969729-789-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-01-15full-release2026-06-01 00:53:00

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
Pentrexcilina Children TOTAL RELIEF Multi-SymptomACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN USP, PHENYLEPHRINE HYDROCHLORIDEOPMX LLC2bc10608-ddba-1e68-e063-6294a90aef672025-01-15WarningsExact identifier
ndc (package): 69729-789-06
ndc (product): 69729-789
ndc11 (package): 69729078906
spl set id: 2bc10608-ddba-1e68-e063-6294a90aef67

Reported adverse events (FAERS/openFDA)#

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