GREEN GUARD MAXIMUM NON-ASPIRIN- 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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Green Guard® Maximum Strength Non-Aspirin

Drug Facts

Active ingredient (in each tablet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

For the temporary relief of minor aches and pains associated with

For the reduction of fever.

Warnings

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

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.
  • for more than 10 days for pain unless directed by a doctor
  • for more than 3 days for fever unless directed by a doctor

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 using and ask a doctor if

  • symptoms do not improve
  • pain or fever persists or gets worse
  • new symptoms occur
  • redness or swelling is present

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of accidental 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

Adults and children: (12 years and older)

Take 2 tablets every 4 to 6 hours as needed. Do not take more than 8 tablets in 24 hours.

Children under 12 years:

Do not give this adult strength product to children under 12 years of age;

this will provide more than the recommended dose (overdose) and may cause liver damage.

Other information

Inactive ingredients

corn starch, hypromellose, maltodextrin*, microcrystalline cellulose*, polyethylene glycol, povidone*, pregelatinized starch*, 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

Compare Active Ingredient To Extra Strength Tylenol®

Green Guard®

Pull Out

Tire Para Abrir

Acetaminophen 500 mg/Acetaminofeno 500 mg

Pain Reliever/Fever Reducer

Alivia el Dolor/Reduce la Fiebre

Tylenol® is a Registered Trademark of McNeil Consumer Products

125 Packets of 2 Tablets

250 Tablets

Order #2222

Distributed by Green Guard® St Louis. MO 63045

An FDA Regulated Facility

Green Guard

GREEN GUARD MAXIMUM NON-ASPIRIN 
acetaminophen tablet, film coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-009
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg
Inactive Ingredients
Ingredient Name Strength
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
Color white (white) Score no score
Shape ROUND (ROUND) Size 12mm
Flavor Imprint Code AZ;235
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:47682-009-33 50 in 1 BOX 12/30/2008
1 NDC:47682-009-99 2 in 1 PACKET; Type 0: Not a Combination Product
2 NDC:47682-009-48 125 in 1 BOX 12/30/2008
2 NDC:47682-009-99 2 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part343 12/30/2008
Labeler - Unifirst First Aid Corporation (832947092)
Establishment
Name Address ID/FEI Business Operations
Prestige Packaging 170837962 relabel(47682-009) , repack(47682-009)

Revised: 4/2019
Document Id: 86a891c7-9e64-df32-e053-2991aa0ad2df
Set id: 30f77d4d-839e-4d96-9f24-0254e6a47b81
Version: 4
Effective Time: 20190416
 
Unifirst First Aid Corporation