OTIS CLAPP BACK QUELL- magnesium salicylate, acetaminophen tablet, film coated 
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Otis Clapp Back Quell

Drug Facts

Active ingredients (in each tablet)

Acetaminophen 200 mg

Magnesium Salicylate U.S.P. (NSAID*) 200 mg

magnesium (total) 13 mg

*nonsteroidal anti-inflammatory drug

Purposes

Pain reliever/fever reducer

Pain reliever/fever reducer

Uses

For the temporary relief of minor aches and pains associated with

  • back pain
  • muscular aches

Warnings

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:

Salicylates (NSAIDs) 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 skin or allergic 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 4,0000 mg of acetaminophen in 24 hours
  • 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 NSAIDs (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

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.
  • for pain for more than 10 days unless directed by a doctor
  • for more than 3 days for fever unless directed by a doctor
  • if you ever have had an allergic reaction to any other pain relievers/ fever reducers
  • right before or after heart surgery
  • if you are taking prescription drugs for gout, diabetes, or arthritis

Ask a doctor before use if

  • stomach bleeding warning applies to you
  • you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
  • you are taking a diuretic
  • you have a history of stomach problems such as heartburn

Ask a doctor or pharmacist before use if you are

  • taking the blood thinning drug warfarin
  • under a doctor's care for any serious condition
  • taking any other drug

When using this product

  • take with food or milk if stomach upset occurs

Stop use and ask a doctor if

  • you experience any of the following signs of stomach bleeding:
  • feel faint
  • vomit blood
  • have bloody or black stools
  • have stomach pain that does not get better
  • symptoms do not improve
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • ringing in the ears or loss of hearing occurs
  • redness or swelling is present in the painful area
  • any new symptoms appears

If pregnant or breast-feeding, ask a health care professional before use. It is especially important not to use salicylates (NSAIDs) during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

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

  • do not use more than directed

Adults and children: (12 years and older)

Take 2 tablets as needed for pain every 6 hours. Do not exceed 8 tablets in 24 hours or as directed by a doctor.

Children under 12 years: Do not give to children under 12 years of age.

Other information

  • each dose contains 26mg of Magnesium
  • tamper evident, do not use if packet is torn, cut or opened.
  • store at controlled room temperature 15º-30ºC (59º to 86ºF)
  • avoid excessive heat and humidity

Inactive ingredients

FD&C Red #28, microcrystalline cellulose, povidone, starch, stearic acid

Questions or comments?

1-800-634-7680

Principal Display Panel - OC Back Quell Label

Otis Clapp

Quality and Integrity Since 1840

BACK QUELL ™

Pain Reliever

Back Pain Relief

Muscles and Sprains

See Warnings and Directions on Side Panel

Acetaminophen 200 mg,

Magnesium Salicylate (NSAID) 200 mg

Tear Out Along Perforation To Dispense

PROFESSIONAL HEALTHCARE

300 Tablets (150 PACKETS OF 2)

OC Back Quell Label

OTIS CLAPP BACK QUELL 
magnesium salicylate, acetaminophen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-587
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM SALICYLATE (UNII: 41728CY7UX) (SALICYLIC ACID - UNII:O414PZ4LPZ) MAGNESIUM SALICYLATE200 mg
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN200 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
D&C RED NO. 28 (UNII: 767IP0Y5NH)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
Colorpink (pink) Scoreno score
ShapeROUND (ROUND) Size12mm
FlavorImprint Code FR;1
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-587-03150 in 1 BOX12/30/200802/01/2022
1NDC:47682-587-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34312/30/200802/01/2022
Labeler - Unifirst First Aid Corporation (832947092)
Establishment
NameAddressID/FEIBusiness Operations
Prestige Packaging080667761relabel(47682-587) , repack(47682-587)

Revised: 6/2021
 
Unifirst First Aid Corporation