ACETAMINOPHEN- acetaminophen tablet 
Bryant Ranch Prepack

----------

Acetaminophen 325 mg Tablets
Regular Strength

Active ingredient (in each tablet)

Acetaminophen 325 mg

Purpose

Pain Reliever/Fever Reducer

Uses

To reduce fever and for the temporary relief of minor aches and pains due to:

•headache

•muscular aches

•backache

•minor pain of arthritis

•the common cold

•toothache

•premenstrual and menstrual cramps.

•Temporarily reduces fever.

Warnings

Liver warning:

This product contains acetaminophen. Severe liver damage may occur if 

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 non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if the user has ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if the user has

  • has liver disease
  • is a child with pain of arthritis

Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin

Stop use and ask a doctor if:

  • pain gets worse or lasts more than 10 days (for adults) or 5 days (for children)
  • fever gets worse or lasts more than 3 days
  • new symptoms occur
  • redness or swelling is present.

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.

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.(1-800-222-1222)

Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions - do not take more than directed (see overdose warning)

 adults & children
12 years and over
  • take 2 tablets every 4 to 6 hours while symptoms last
  • do not take more than 10 tablets in 24 hours
  • do not use for more than 10 days unless directed by a doctor
 children 6-11 years
  •  take 1 tablet every 4 to 6 hours while symptoms last
  • do not take more than 5 tablets in 24 hours
  • do not use for more than 5 days unless directed by a doctor
 child under 6 years ask a doctor

Other information

Inactive Ingredients:

Gelatinized starch, magnesium stearate, povidone

Questions or Comments?

Call toll-free 1-877-225-6999

Manufactured for
Akron Pharma, Inc.,

373 RT US46 W Building E,

Suite 117, Fairfeld, NJ - 07004

Mfg. Lic. No: TN/DRUGS/558/1997

* This product is not manufactured or distributed by Johnson and Johnson, consumer inc., distributor of regular Tylenol Tablets.

HOW SUPPLIED

Acetaminophen 325 mg tablet: white color, round shape and the imprint code is A325. 

NDC: 71335-2747-1: 20 Tablets in a BOTTLE

NDC: 71335-2747-2: 100 Tablets in a BOTTLE

NDC: 71335-2747-3: 30 Tablets in a BOTTLE

NDC: 71335-2747-4: 2 Tablets in a BOTTLE

NDC: 71335-2747-5: 6 Tablets in a BOTTLE

NDC: 71335-2747-6: 10 Tablets in a BOTTLE

NDC: 71335-2747-7: 60 Tablets in a BOTTLE

NDC: 71335-2747-8: 90 Tablets in a BOTTLE

NDC: 71335-2747-9: 40 Tablets in a BOTTLE

NDC: 71335-2747-0: 24 Tablets in a BOTTLE

Store at 20° to 25°C (68° to 77°F)

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

Acetaminophen 325 mg Tablet

Label
ACETAMINOPHEN 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-2747(NDC:71399-1025)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
Product Characteristics
ColorwhiteScore2 pieces
ShapeROUNDSize4mm
FlavorImprint Code A325
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71335-2747-120 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
2NDC:71335-2747-2100 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
3NDC:71335-2747-330 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
4NDC:71335-2747-42 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
5NDC:71335-2747-56 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
6NDC:71335-2747-610 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
7NDC:71335-2747-760 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
8NDC:71335-2747-890 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
9NDC:71335-2747-940 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
10NDC:71335-2747-024 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01312/06/2024
Labeler - Bryant Ranch Prepack (171714327)
Registrant - Bryant Ranch Prepack (171714327)
Establishment
NameAddressID/FEIBusiness Operations
Bryant Ranch Prepack171714327REPACK(71335-2747) , RELABEL(71335-2747)

Revised: 10/2025
Document Id: d0a7080b-29dc-4e43-99e1-9027a3bbd1cd
Set id: 8e40f8f1-03c5-444b-8b5e-4532c3146e47
Version: 1
Effective Time: 20251002
 
Bryant Ranch Prepack