FDA.reportPublic FDA data

MAX relief junior Cherry flavor

Manufacturer
Akron Pharma Inc.
Effective date
2026-08-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-09-03 03:01:40

Label at a glance#

ProductMAX relief junior
Active ingredientACETAMINOPHEN
Label structure8 sections

Indications and uses

temporarily: reduces fever relieves minor aches and pains due to: the common cold flu headache sore throat toothache

Dosage and administration

this product does not contain directions or complete warnings for adult use shake well before using mL = milliliter find right dose on chart below. if possible, use weight to dose, otherwise use age  use only the enclosed dosing cup designed for use with product.  Weight (lbs)  Age (yrs.)  Dose (tsp or mL) Weight (lbs)   Age (yrs.) Dose (tsp or mL)   under 24  under 2  ask a doctor  48 to 59  6 to 8  2 tsp or 10 m...

Storage and handling

Store at room temperature 20°-25°C (68°-77°F). Protect from freezing. Protect from light.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient(in each 5mL)                                             Purpose
Acetaminophen 160 mg ………………………….........Pain reliever/fever reducer

Uses

OTC - PURPOSE SECTION

temporarily: reduces fever

relieves minor aches and pains due to:

  • the common cold
  • flu
  • headache
  • sore throat
  • toothache

Warnings

WARNINGS SECTION

Liver Warning: This product contains acetaminophen. Severe liver damage may occur if your child takes:

  • more then 5 doses in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen

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, persist or more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

Do not use

  • 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 your child is allergic to acetaminophen or anyof the inactive ingredients in this product.

Ask a doctor or pharmacist before use if the child has

OTC - ASK DOCTOR SECTION

liver disease.

Ask  doctor or pharmacist before use if your child is 

INDICATIONS & USAGE SECTION

taking the blood thinning drug warfarin. When using this product do not exceed recommended dose (see overdose warning)

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • pain gets worse or lasts for more then 5 days
  • fever gets worse or last for more then 3 days
  • new symptoms occur redness or swelling is present. These could be signs of a serious condition. 
Overdose warning:

SPL UNCLASSIFIED SECTION

In case of overdose, get medical help to contact Poison Control Center (1-800-222-1222) right away. Quick medical attention is critical even if you do not notice any signs or symptoms.

Keep out of Reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

  • this product does not contain directions or complete warnings for adult use
  • shake well before using
  • mL = milliliter
  • find right dose on chart below. if possible, use weight to dose, otherwise use age 
  • use only the enclosed dosing cup designed for use with product.
 Weight (lbs) Age (yrs.) Dose (tsp or mL)Weight (lbs)  Age (yrs.)Dose (tsp or mL) 
 under 24 under 2 ask a doctor 48 to 59 6 to 8 2 tsp or 10 mL
 25 to 35 2 to 3 1 tsp or 5 mL 60 to 71 9 to 10 2 1/2 tsp or 12.5 mL
 36 to 47 4 to 5 1 1/2 tsp or 7.5 mL 72 to 95 11 2 1/2 tsp or 12.5 mL

Other Information

STORAGE AND HANDLING SECTION

  • Store at room temperature 20°-25°C (68°-77°F). Protect from freezing. Protect from light.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Anhydrous Citric Acid, Cherry Flavor, Glycerin, Microcrystalline cellulose and Sodium Methyl Cellulose, Potassium Sorbate, Purified Water, Sorbitol, Sucralose, Sucrose, Xanthan gum.

Questions or comments?

OTC - QUESTIONS SECTION

call toll-free 1-877-225-6999

Manufactured for:

Akron Pharma, Inc.

Fairfield, NJ 07004

www.akronpharma.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334455

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71399-0038-4ML - Milliliter71399-003829afcbf4-0997-429a-90a7-04941d424fc412024-06-10
71399-0038-6ML - Milliliter71399-0038ec196839-af1a-41e5-ba7b-ae1210b070d812024-06-10
71399-0038-8ML - Milliliter71399-0038e7c8d9e8-9616-4443-bbde-97ce6850795112024-06-10

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71399-003871399-0038-4, 71399-0038-8, 71399-0038-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACETAMINOPHEN362O9ITL9DACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
GLYCERINPDC6A3C0OXIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
SORBITOL506T60A25RIACT
SUCRALOSE96K6UQ3ZD4IACT
SUCROSEC151H8M554IACT
XANTHAN GUMTTV12P4NEEIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-10-27full-release2026-06-01 01:41:02
22024-04-28full-release2026-06-01 00:11:37

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
MAX relief juniorCHILDREN ACETAMINOPHENAkron Pharma Inc.d7874e4d-0b38-4bb1-9a62-aa4f66d9baf92026-08-31WarningsExact identifier
ndc (package): 71399-0038-6
ndc (package): 71399-0038-8
ndc (package): 71399-0038-4
ndc (product): 71399-0038
ndc11 (package): 71399003806
ndc11 (package): 71399003808
ndc11 (package): 71399003804
spl id: 5a61309c-0801-fd53-e063-6394a90a3108
spl set id: d7874e4d-0b38-4bb1-9a62-aa4f66d9baf9

Reported adverse events (FAERS/openFDA)#

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