Acetaminophen - Bryant Ranch Prepack

Manufacturer
Bryant Ranch Prepack
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:34

Label at a glance#

ProductAcetaminophen
Active ingredientACETAMINOPHEN
Label structure13 sections

Indications and uses

To reduce fever and for the temporary relief of minor aches and pains due to: headache  muscular aches backache minor pain from arthritis  the common cold toothache premenstrual and menstrual cramps temporarily reduces fever.

Dosage and administration

Do not take more than directed Adults and 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 take for more than 10 days unless directed by a doctor Children 6 years to under 12 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 b...

Label contents#

Full prescribing information#

DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING. Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each tablet)                          Purpose
Acetaminophen USP, 325 mg.................................Pain Reliever/Fever Reducer

Uses

INDICATIONS & USAGE SECTION

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

  • headache 
  • muscular aches
  • backache
  • minor pain from arthritis 
  • the common cold
  • toothache
  • premenstrual and menstrual cramps
  • temporarily reduces fever.

Warnings

WARNINGS SECTION

Liver warning: This product contains acetaminophen.

Severe liver damage may occur if

  • adult takes more than 10 tablets in 24 hours, which is the maximum daily amount 
  • child takes more than 5 tablets in 24 hours 
  • taken with other drugs containing acetaminophen
  • adult has 3 or more alcoholic drinks every day while using this product

Do not use

OTC - DO NOT USE SECTION

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you are allergic to acetaminophen or any of the inactive ingredients in this product.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have liver disease.

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
Stop use and ask a doctor if
• pain gets worse or lasts more than 10 days in adults and children.
• pain gets worse or lasts more than 5 days in children under 12 years.
• 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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Do not take more than directed
Adults and 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 take for more than 10 days unless directed by a doctor

Children 6 years to under 12 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

Children under 6 years:
ask a doctor

Other Information

  • SODIUM FREE
  • store at 25°C (77°F) excursions permitted between 15°-30°C (59°-86°F)
  • see end panel for lot number and expiration date.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, stearic acid, talc, titanium dioxide.

OTC - QUESTIONS SECTION

Questions and Comments? Call 1-844-474-7464

Distributed by:

Rising Pharma Holdings, Inc.

East Brunswick, NJ 08816

Made in India

Mfg. Lic. No.: G/25/2258

Issued: 06/2025 (S-065)

Issued: 07/2025 (S-069-00)

†This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division, owner of the registered trademark Tylenol® Regular strength.

HOW SUPPLIED

How Supplied Section

Acetaminophen 325mg Tablets

  • NDC 71335-3130-1: 20 Tablets in a BOTTLE
  • NDC 71335-3130-2: 100 Tablets in a BOTTLE
  • NDC 71335-3130-3: 30 Tablets in a BOTTLE
  • NDC 71335-3130-4: 2 Tablets in a BOTTLE
  • NDC 71335-3130-5: 6 Tablets in a BOTTLE
  • NDC 71335-3130-6: 10 Tablets in a BOTTLE
  • NDC 71335-3130-7: 60 Tablets in a BOTTLE
  • NDC 71335-3130-8: 90 Tablets in a BOTTLE
  • NDC 71335-3130-9: 40 Tablets in a BOTTLE
  • NDC 71335-3130-0: 24 Tablets in a BOTTLE

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Acetaminophen 325mg Tablets

Label
Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313782acetaminophen 325 MG Oral TabletPSN1
313782acetaminophen 325 MG Oral TabletSCD1
313782APAP 325 MG Oral TabletSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeData Matrix(01)00371335313012(21)0123456789(17)280508(10)208820GTIN-14: 00371335313012
GTIN-12: 371335313012
UPC-A: 371335313012
EAN-13: 0371335313012
GTIN storage (14 digits): 00371335313012
lbl713353130.jpg
QR code linkQR Codedailymed.nlm.nih.gov/dailymed/search.cfm?adv=1&query=NDC:71335-3130-1lbl713353130.jpg
Data codeCode 1287133531301lbl713353130.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-3130-0Acetaminophen24 in 1 BOTTLETABLET, FILM COATED241
71335-3130-1Acetaminophen20 in 1 BOTTLETABLET, FILM COATED201
71335-3130-2Acetaminophen100 in 1 BOTTLETABLET, FILM COATED1001
71335-3130-3Acetaminophen30 in 1 BOTTLETABLET, FILM COATED301
71335-3130-4Acetaminophen2 in 1 BOTTLETABLET, FILM COATED21
71335-3130-5Acetaminophen6 in 1 BOTTLETABLET, FILM COATED61
71335-3130-6Acetaminophen10 in 1 BOTTLETABLET, FILM COATED101
71335-3130-7Acetaminophen60 in 1 BOTTLETABLET, FILM COATED601
71335-3130-8Acetaminophen90 in 1 BOTTLETABLET, FILM COATED901
71335-3130-9Acetaminophen40 in 1 BOTTLETABLET, FILM COATED401

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57237-346-01EA - Each57237-3462ccb0212-ce31-48f1-bb7c-e48bd05936bd12025-08-11
57237-346-10EA - Each57237-34639d36403-64f2-4dbf-ad05-c27fd026367a12025-11-13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetaminophenACETAMINOPHENBryant Ranch Prepack816b65d7-e53f-44c4-a418-074279d4b2af2026-05-08WarningsExact identifier
ndc (package): 71335-3130-2
ndc (package): 71335-3130-0
ndc (package): 71335-3130-1
ndc (package): 71335-3130-3
ndc (package): 71335-3130-5
ndc (package): 71335-3130-6
ndc (package): 71335-3130-9
ndc (package): 71335-3130-7
ndc (package): 71335-3130-8
ndc (package): 71335-3130-4
ndc (product): 71335-3130
ndc11 (package): 71335313006
ndc11 (package): 71335313003
ndc11 (package): 71335313000
ndc11 (package): 71335313001
ndc11 (package): 71335313007
ndc11 (package): 71335313004
ndc11 (package): 71335313005
ndc11 (package): 71335313002
ndc11 (package): 71335313009
ndc11 (package): 71335313008
spl id: 7db1fd81-3443-4722-9a1b-497eace4d3c4
spl set id: 816b65d7-e53f-44c4-a418-074279d4b2af

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.