PERCOGESIC EXTRA STRENGTH- acetaminophen and diphenhydramine capsule, coated 
Medtech Products Inc.

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Percogesic Extra Strength 63029-054

Drug Facts

Active Ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Active Ingredient (in each caplet)

Diphenhydramine HCl 12.5 mg

Purpose

Antihistamine

Uses:

for temporary relief of minor aches and pains due to:

Temporarily relieves

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

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • with any other product containing diphenhydramine, even one used on skin
  • If you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

  • liver disease
  • a breathing problem such as emphysema or chronic bronchitis
  • trouble urinating due to an enlarged prostate gland
  • glaucoma

Ask a doctor or pharmacist before use if your are

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers

When using this product

  • marked drowsiness may occur
  • avoid alcoholic beverages
  • alcohol, sedatives, and tranquilizers may cause drowsiness
  • may cause excitability, especially in children
  • be careful driving a motor vehicle or operating machinery.

Stop use and ask a doctor if

  • pain persists for more than 10 days
  • fever persists for more than 3 days (unless directed by a doctor)
  • condition worsens or new symptoms occur
  • redness or swelling is present.

These may be signs of a serious condition.

If you are pregnant or breast-feeding,

ask a health professional before use.

Keep out of the reach of children.

Overdose warning: Taking more than the recommended dose (overdose) could cause serious health problems, including liver damage. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Do not exceed recommended dosage.

Directions

Adults and children 12 years of age and older: take 2 caplets every 6 hours. Maximum daily dose is 6 tablets. Children under 12 years of age: ask a doctor.

Other information

Inactive ingredients

croscarmellose sodium, FD&C yellow no. 6 lake, hypromellose, magnesium stearate, microcrystalline cellulose, mineral oil, polyvinylpyrrolidone, silica, sodium carboxymethyl starch, starch, stearic acid, talc, titanium dioxide, triacetin

Questions?

1-800-443-4908

PRINCIPAL DISPLAY PANEL

EXTRA STRENGTH
Percogesic®
Acetaminophen/

Diphenhydramine



Fever Reducer/ Antihistamine


40 COATED CAPLETS

PRINCIPAL DISPLAY PANEL
EXTRA STRENGTH
Percogesic®
Acetaminophen/
Diphenhydramine


Fever Reducer/ Antihistamine

40 COATED CAPLETS

PERCOGESIC  EXTRA STRENGTH
acetaminophen and diphenhydramine capsule, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-054
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
DIPHENHYDRAMINE (UNII: 8GTS82S83M) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE12.5 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
MINERAL OIL (UNII: T5L8T28FGP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
Product Characteristics
Colororange (peach colored) Scoreno score
ShapeCAPSULESize10mm
FlavorImprint Code ES;PER
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-054-601 in 1 CARTON07/07/2010
160 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:63029-054-401 in 1 CARTON07/07/2010
240 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01307/07/2010
Labeler - Medtech Products Inc. (122715688)

Revised: 2/2024
Document Id: dd068345-eb74-40b1-80b5-ef9df6fde1cd
Set id: 2c5f1140-fb83-42c9-b0b1-5e2bd69340bb
Version: 1
Effective Time: 20240201
 
Medtech Products Inc.