Zee Painaid Back Relief Formula

Manufacturer
Cintas Corp | UltraTab Labratories
Effective date
2022-02-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:07:15

Label at a glance#

ProductZee Painaid Back Relief Formula
Active ingredientMAGNESIUM SALICYLATE, ACETAMINOPHEN, CAFFEINE
Label structure15 sections

Dosage and administration

adults: take 2 tablets every 6 hours, not more than 8 tablets in 24 hours children under 12 years: ask a doctor

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (in each tablet)

OTC - PURPOSE SECTION

Acetaminophen 250 mg
Caffine 50 mg
Magnesium salicylate 290 mg (NSAID*)
*nonsteroidal anti-inflammatory

Purpose

OTC - PURPOSE SECTION

Pain reliever

Adjuvant

Pain reliever

INDICATIONS & USAGE SECTION

Use temporarily relieves minor back pain

Warnings

WARNINGS SECTION

Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

Allergy alert: Magnesium salicylate may cause a severe allergic reaction which may include:

  • hives
  • facial swelling
  • asthma (wheezing)
  • shock

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

  • skin reddening
  • blisters
  • rash

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

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

  • more than 8 tablets in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding.  The chance is higher if you

  • are age 60 or older
  • have had stomach ulcers or bleeding problems
  • take a blood thinning (anticoagulant) or steroid drug
  • take other drugs containing prescription or nonprescription NDAIDs (aspirin, ibuprofen, naproxen, or others)
  • have 3 or more alcoholic drinks every day while using this product
  • take more or for a longer time than directed

Caffeine warning: The recommended dose of this product contains about as much caffeine as a cup of coffee.  Limit the use of caffeine-containing medications, foods, or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and occasionally rapid heart beat

Do not use

OTC - DO NOT USE SECTION

  • with any other drug containing acetaminophen (prescription or nonprescription)) this will provide more than the recommended dose (overdose) of acetaminophen and could cause serious health concerns.
  • with any other pain reliver/fever reducer
  • if you have ever had an allergic reaction to any other pain reliever/fever reducer
  • for pain for more than 10 days or for fever for more than 3 days unless directed by a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have:

  • stomach problems (such as heartburn, upset stomach or stomach pains)
  • stomach bleeding warning applies to you
  • gastric ulcers
  • bleeding problems
  • you have asthma, high blood pressure, heart disease, liver disease, or kidney disease
  • you are taking a diuretic

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking a prescription drug for anticoagulation (thinning of blood), diabetes, gout, or arthritis. When using this product do not exceed recommended dose. Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

OTC - STOP USE SECTION

​Stop use and ask doctor if:​

  • ringing in the ears or loss of hearing occurs
  • pain or fever persists or gets worse
  • ​new symptoms occur
  • redness or swelling is present
  • you feel faint, vomit blood or have bloody or black stools, have stomach pain that does not get better. These are signs of stomach bleeding
  • an allergic reaction occurs. Seek medical help right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

​If pregnant or breast-feeding, ask a health professional before use. IT IS ESPECIALLY IMPORTANT NOT TO USE MAGNESIUM SALICYLATE DURING THE LAST 3 MONTHS OF PREGNANCY UNLESS SPECIFICALLY DIRECTED TO DO SO BY A DOCTOR BECAUSE IT MAY CAUSE PROBLEMS IN THE UNBORN CHILD OR COMPLICAITONS DURING DELIVERY.​

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.  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

  • adults: take 2 tablets every 6 hours, not more than 8 tablets in 24 hours
  • children under 12 years: ask a doctor

Other information

OTHER SAFETY INFORMATION

  • ​each tablet contains:​ magnesium 24 mg
  • store at 15-30°C (59-86°F)
  • avoid excessive heat above 40°C (104°F)
  • Tamper Evident. Do not use if packet is torn or open

INACTIVE INGREDIENT SECTION

Inactive ingredients​ hydroxypropyl methylcellulose, maltodextrin, microcrystalline cellulose, polyethylene glycol, povidone, starch, stearic acid, titanium dioxide

SPL UNCLASSIFIED SECTION

Questions? 1-800-327-2704 Monday-Friday 8:00-5:00PM

SPL UNCLASSIFIED SECTION

For industrial use only. Not for retail sale./Solo para uso industrial. No apto venta al por menor.

Distributed by/Distribuido por ​ZEE Medical Distributors, LLC ​Mason, OH 45040

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Back Relief Formula

Acetaminophen/Magnesium Salicylate (NSAID)/Caffeine

Pain Reliever

See new warnings information

100 Tablets (2 Tablets per Packet)

Distributed by ZEE Medical Distributors, LLC Mason, OH 45040

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42961-02742961-027-01

Ingredients#

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

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

Source Document#

Source XML

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
fb02669b-fa2b-4a73-8d83-43e6d4509c59f4b05683-4c0d-400f-baca-bbcdc6afcc8f2022-12-27WarningsExact identifier
spl set id: f4b05683-4c0d-400f-baca-bbcdc6afcc8f

Reported adverse events (FAERS/openFDA)#

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