EXTRA STRENGTH PAIN RELIEF- acetaminophen tablet 
Geri-Care Pharmaceutical Corp

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gc221

Active ingredient

Acetaminophen 500 mg

Purpose

Pain Reliever/Fever Reducer

Uses

Warnings

Liver warning:

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

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

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

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. 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

Other Information

Inactive ingredients

povidone, sodium starch glycolate, starch, stearic acid.

Questions or comments?

1-800-540-3765

Package label

1

EXTRA STRENGTH PAIN RELIEF 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57896-221
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (WHITE) Scoreno score
ShapeCAPSULE (Capsule) Size15mm
FlavorImprint Code M2A457344
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57896-221-01100 in 1 BOTTLE; Type 0: Not a Combination Product12/01/2011
2NDC:57896-221-101000 in 1 BOTTLE; Type 0: Not a Combination Product11/01/2011
3NDC:57896-221-0550 in 1 BOTTLE; Type 0: Not a Combination Product11/01/2013
4NDC:57896-221-25250 in 1 BOTTLE; Type 0: Not a Combination Product01/01/201701/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01301/01/1989
Labeler - Geri-Care Pharmaceutical Corp (611196254)
Registrant - Geri-Care Pharmaceutical Corp (611196254)

Revised: 10/2023
Document Id: 0761fb5a-1cc0-a6a1-e063-6294a90a29af
Set id: ae00015d-5e5f-4099-ba03-b20bf45ed374
Version: 5
Effective Time: 20231010
 
Geri-Care Pharmaceutical Corp