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

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gc 102

Active Ingredients

Acetaminophen 325 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:

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

REGULAR STRENGTH PAIN RELIEF 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57896-102
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 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
ColorwhiteScoreno score
ShapeROUNDSize10mm
FlavorImprint Code GC101
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57896-102-01100 in 1 BOTTLE; Type 0: Not a Combination Product12/01/2011
2NDC:57896-102-101000 in 1 BOTTLE; Type 0: Not a Combination Product01/01/2012
3NDC:57896-102-0550 in 1 BOTTLE; Type 0: Not a Combination Product12/01/2011
4NDC:57896-102-20200 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2018
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: 07ee2cb2-70df-6b8a-e063-6394a90a3e97
Set id: 6158e954-32d8-4718-e053-2a91aa0a27f3
Version: 6
Effective Time: 20231017
 
Geri-Care Pharmaceutical Corp