EXTRA STRENGTH PAIN RELIEF- acetaminophen tablet, coated 
Chain Drug Consortium, LLC

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premier value 251

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

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.

Overdose Warning: Taking more than the recommended dose (overdose) may cause liver damage. 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.

Keep out of reach of children.

Directions

Other Information

Inactive Ingredients

croscarmellose sodium, D&C Red #33, FD&C Blue #1, FD&C Red #40, gelatin, hydroxypropyl cellulose, hypromellose, iron oxide, PEG, povidone, propylene glycol, shellac glaze, starch, stearic acid, titanium dioxide.

package label

NDC 68016-029-47

Compare to active ingredient in Extra Strength Tylenol Rapid Release Gels*

Extra Strength

PAIN RELIEF

ACETAMINOPHEN

Rapid Release

Pain Reliever/ Fever Reducer

Gelcaps

400 Gelcaps

500 mg each

251 label

EXTRA STRENGTH PAIN RELIEF 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-029
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GELATIN (UNII: 2G86QN327L)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
SHELLAC (UNII: 46N107B71O)  
Product Characteristics
Colorred (with blue and a gray band) Scoreno score
ShapeCAPSULE (Gelcap) Size19mm
FlavorImprint Code L;5
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-029-201 in 1 CARTON09/01/2007
1100 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:68016-029-141 in 1 CARTON09/01/200708/31/2022
250 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:68016-029-47400 in 1 BOTTLE; Type 0: Not a Combination Product09/01/200704/30/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01309/01/2007
Labeler - Chain Drug Consortium, LLC (101668460)
Registrant - Geri-Care Pharmaceutical Corp (611196254)

Revised: 10/2023
Document Id: 08156ef8-87e0-ec67-e063-6394a90a4f87
Set id: 05e11584-1876-0207-e054-00144ff88e88
Version: 5
Effective Time: 20231019
 
Chain Drug Consortium, LLC