GREEN GUARD MAXIMUM NON-ASPIRIN- acetaminophen tablet, film coated 
Unifirst First Aid Corporation

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Green Guard® Maximum Strength Non-Aspirin

Drug Facts

Active ingredient (in each tablet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

temporarily relieves minor aches and pains due to:

temporarily reduces fever

Warnings

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

■ more than 4,000 mg 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

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.

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 you are allergic to acetaminophen or any of the inactive ingredients in this product

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 for more than 10 days
  • fever gets worse or lasts more than 3 days
  • new symptoms occur
  • redness or swelling is present

These could be signs of a serious condition.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.I

Overdose Warning:

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

Directions

Adults and children: (12 years and over) ■ take 2 tablets every 6 hours while symptoms last.
■ do not take more than 6 tablets in 24 hours, unless directed by a doctor

■ do not use for more than 10 days unless directed by a doctor

Children under 12 years: Ask a doctor

Other information

Inactive ingredients

corn starch*, hypromellose*, polyethylene glycol*, povidone (K-30)*, pregelatinized starch*, purified water*, sodium starch glycolate*, stearic acid*, titanium dioxide*

* m ay contain

Questions or comments? 1-800-869-6970

Green Guard Max Non-Aspirin Label

Maximum Strength Non-Aspirin relief™

Acetaminophen 500 mg/Acetaminofeno 500 mg

Pain Reliever/Fever Reducer

Alivia el Dolor/Reduce la Fiebre

Compare Active Ingredient To Extra Strength Tylenol®

Green Guard®

Pull Out

Tire Para Abrir

Tylenol® is a Registered Trademark of McNeil Consumer Products

50 Packets of 2 Tablets

100 Tablets

Order #2224

Distributed by Green Guard® St Louis. MO 63045

175R 2224 11-6-23 AH

GREEN GUARD MAXIMUM NON-ASPIRIN 
acetaminophen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-009
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES (UNII: 3NXW29V3WO)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size12mm
FlavorImprint Code AZ;235
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-009-3350 in 1 BOX12/30/2008
1NDC:47682-009-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-009-48125 in 1 BOX12/30/2008
2NDC:47682-009-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01312/30/2008
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 2/2024
Document Id: 1066bebe-871b-a180-e063-6394a90a9ac0
Set id: 30f77d4d-839e-4d96-9f24-0254e6a47b81
Version: 12
Effective Time: 20240202
 
Unifirst First Aid Corporation