Active Ingredient (in each 0.85 oz Pouch) Purpose

Manufacturer
MOREMED INC. | Catalent Pharma Solutions, LLC
Effective date
2026-08-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-08 02:01:29

Label at a glance#

ProductMantra Pain Gel raspberry
Active ingredientACETAMINOPHEN
Label structure12 sections

Indications and uses

Temporarily relieves minor aches and pains due to: headache  minor pain of arthritis  backache  the common cold  temporarily reduces fever  muscular aches  premenstrual and menstrual cramps  toothache

Dosage and administration

Do not exceed 2 pouches in 24 hours unless directed by a doctor. Adults and children 12 years and over : take 1 pouch every 12 hours while symptoms last. Do not use for more than 10 days, unless directed by a doctor. Children under 12 years : do not use.

Label contents#

Full prescribing information#

Active Ingredient (in each 0.85 oz Pouch)               Purpose

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 500 mg                                           Pain reliever

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains due to:

  • headache 
  • minor pain of arthritis 
  • backache 
  • the common cold 
  • temporarily reduces fever 
  • muscular aches 
  • premenstrual and menstrual cramps 
  • toothache

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 (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • 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.

OTC - DO NOT USE SECTION

Do not use

  • with any other drug containing acetaminophen
  • if you are allergic to acetaminophen or any of the inactive ingredients in this product

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • liver disease 

Ask a doctor or pharmacist before use if you
are•taking the blood thinning drug warfarin

  • Stop use and ask a doctor if
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • new symptoms occur
  • redness or swelling is present

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. Quick 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 exceed 2 pouches in 24 hours unless directed by a doctor.
  • Adults and children 12 years and over: take 1 pouch every 12 hours while symptoms last.
  • Do not use for more than 10 days, unless directed by a doctor.
  • Children under 12 years: do not use.

Other information

SPL UNCLASSIFIED SECTION

  • Store at controlled room temperature 
  • Avoid excessive heat above 40°C (104°F). 
  • Protect from moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ascorbic Acid, Citric Acid, Glycerin, Manuka Honey, Natural Raspberry Flavor, Pectin, Purified Water, Sodium Citrate

Questions or comments?

SPL UNCLASSIFIED SECTION

Call 1-800-529-3182 (toll-free)

Mon–Fri 9 AM–5 PM EST

SPL UNCLASSIFIED SECTION

Ask a doctor before use if you have diabetes.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85410-05085410-050-02

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
Mantra Pain Gel raspberryACETAMINOPHENMOREMED INC.7c8bdf49-a6d2-4e42-b006-375f103fd0ac2026-08-05WarningsExact identifier
ndc (package): 85410-050-02
ndc (product): 85410-050
ndc11 (package): 85410005002
spl id: 584f5a99-35fb-2dd9-e063-6394a90aae50
spl set id: 7c8bdf49-a6d2-4e42-b006-375f103fd0ac

Reported adverse events (FAERS/openFDA)#

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