Good Neighbor Daytime flu Relief Max Strength Drug facts

Manufacturer
AMERISOURCE BERGEN
Effective date
2026-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:58:18

Label at a glance#

ProductGOOD NEIGHBOR PHARMACY DAYTIME FLU RELIEF MAX STRENGTH
Active ingredientACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE
Label structure9 sections

Indications and uses

▪ temporarily relieves these symptoms due to a common cold or flu: ▪ headache ▪ minor aches and pains ▪ cough due to minor throat and bronchial irritation ▪ minor sore throat pain ▪ temporarily reduces fever

Dosage and administration

• do not use more than directed • take every 6 hours, while symptoms persist • do not take more than 3 packets in 24 hours unless directed by a doctor   Age   Dose   adults and children 12 years of age and over   One packet   children under 12 years of age   do not use ▪ dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume the entire drink within 10-15 minutes. ▪ if using a microwave, add c...

Label contents#

Full prescribing information#

Active ingredients (in each packet)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 1000 mg

Dextromethorphan HBr 30 mg

Purposes

OTC - PURPOSE SECTION

Pain reliever/Fever reducer

Cough suppressant

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves these symptoms due to a common cold or flu:
    • headache
    • minor aches and pains
    • cough due to minor throat and bronchial irritation
    • minor sore throat pain
  • temporarily reduces fever

Warnings

WARNINGS SECTION

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

  • more than 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

Allergy alert: 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: 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

  • in a child under 12 years of age
  • if you are allergic to acetaminophen
  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • 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
  • a breathing problem such as emphysema or chronic bronchitis
  • cough that occurs with too much phlegm (mucus)
  • cough that lasts or is chronic such as occurs with smoking, asthma or emphysema

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • taking the blood thinning drug warfarin

When using this product

OTC - WHEN USING SECTION

  • do not exceed recommended dosage.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • pain 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 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

In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not use more than directed
  • take every 6 hours, while symptoms persist
  • do not take more than 3 packets in 24 hours unless directed by a doctor
  1. Age
  1. Dose
  1. adults and children 12 years of age and over
  1. One packet
  1. children under 12 years of age
  1. do not use
  • dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume the entire drink within 10-15 minutes.
  • if using a microwave, add contents of one packet to 8 oz. of cool water: sip briskly before and after heating.
  • do not overheat.

Other information

SPL UNCLASSIFIED SECTION

  • each packet contains: potassium 6 mg
  • store at room temperature. Protect from excessive heat and moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

anhydrous citric acid, caramel, flavors, maltodextrin, potassium chloride, silica, sucralose, sucrose

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

*Compare to the active ingredients in Theraflu Multi-Symptom Flu Relief Max Strength** Daytime*

NDC 46122-841-59

GOOD NEIGHBOR PHARMACY®

DAYTIME

FLU RELIEF

Max Strength**

Multi-Symptom

Acetaminophen - Pain Reliever/Fever Reducer

Dextromethorphan HBr - Cough Suppressant

Hot liquid therapy that relieves:

  • Fever
  • Body ache
  • Headache
  • Sore throat
  • Cough

Honey Lemon

Natural & Artificial Flavored

**Maximum Strength per 6 hour dose

6 PACKETS

USE AS DIRECTED

*This product is not manufactured or distributed by Haleon group, distributor of Theraflu Multi-Symptom Flu Relief Max Strength Daytime.

TAMPER EVIDENT: DO NOT USE INNER SEALED PACKET IF TORN OR BROKEN

READ ALL WARNINGS AND DIRECTIONS ON CARTON BEFORE USE.

KEEP CARTON FOR REFERENCE. DO NOT DISCARD.

Distributed by: Amerisource Bergen

1 West First Avenue

Conshohocken, PA 19428

Questions or concerns?

www.mygnp.com

ABC Daytime Multi-Symptom Flu Relief Max Strength 6 Packets
ABC Daytime Multi-Symptom Flu Relief Max Strength 6 Packets

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2636656acetaminophen 1000 MG / dextromethorphan hydrobromide 30 MG Powder for Oral SolutionPSN1
2636656acetaminophen 1000 MG / dextromethorphan hydrobromide 30 MG Powder for Oral SolutionSCD1
2636656acetaminophen 1000 MG / dextromethorphan hydrobromide 30 MG Granules for Oral SolutionSY1
2636656APAP 1000 MG / dextromethorphan hydrobromide 30 MG Powder for Oral SolutionSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46122-841-59GOOD NEIGHBOR PHARMACYDAYTIME FLU RELIEF MAX STRENGTH1 in 1 PACKETPOWDER, FOR SOLUTION11
46122-841-59GOOD NEIGHBOR PHARMACYDAYTIME FLU RELIEF MAX STRENGTH6 in 1 CARTONPOWDER, FOR SOLUTION61

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46122-84146122-841-59

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

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
GOOD NEIGHBOR PHARMACY DAYTIME FLU RELIEF MAX STRENGTHACETAMINOPHEN, DEXTROMETHORPHAN HBRAMERISOURCE BERGEN45dc9dd7-134a-4e70-a07e-7bfdf0dc1c4e2026-05-21WarningsExact identifier
ndc (package): 46122-841-59
ndc (product): 46122-841
ndc11 (package): 46122084159
spl id: 45dc9dd7-134a-4e70-a07e-7bfdf0dc1c4e
spl set id: 45dc9dd7-134a-4e70-a07e-7bfdf0dc1c4e

Reported adverse events (FAERS/openFDA)#

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