FDA.reportPublic FDA data

Acetaminophen Oral Solution

Manufacturer
Cardinal Health
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:26:30

Label at a glance#

ProductAcetaminophen Oral Solution
Active ingredientACETAMINOPHEN
Label structure11 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each 5 mL cup) ‑ Purpose Acetaminophen USP 160 mg…………………………..………………..Pain reliever / fever reducer

Purpose

OTC - PURPOSE SECTION

Pain reliever / fever reducer

Acetaminophen 160 mg / 5 mL Unit Dose Cup

DOSAGE & ADMINISTRATION SECTION

Directions

Do not use more than directed Shake well before use

Age (yr)

Dose (mL)

adults

  • take 20 mL (640 mg) every 4 to 6 hours
  • not to exceed 6 doses in a 24-hour period
  • do not use more than 10 days unless directed by a doctor

under 18 years of age

  • ask a doctor

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Warnings and Precautions

WARNINGS AND PRECAUTIONS SECTION

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.

- if you are allergic to acetaminophen or any other inactive ingredients in this product

Warnings

WARNINGS SECTION

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

Do Not Use

OTC - DO NOT USE SECTION

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.

- if you are allergic to acetaminophen or any other inactive ingredients in this product

Ask Doctor

OTC - ASK DOCTOR SECTION

- has liver disease - is pregnant or breast-feeding

Ask Doctor/Pharmacist

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if:
- pain gets worse or lasts more than 10 days - new symptoms occur

- fever gets worse or lasts more than 3 days - redness or swelling is present

These could be signs of a serious condition

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients cherry flavor, citric acid, glycerin, methylcellulose, microcrystalline cellulose, propyl paraben, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xantham gum

Indications and Usage

INDICATIONS & USAGE SECTION

Uses temporarily relieves minor aches and pains due to:

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

Generic Section

SPL UNCLASSIFIED SECTION

Other Information

- store at 20°-25°C (68°-77°F). Avoid excessive heat 40°C (104°F)

- protect from excessive moisture - do not use if lid seal is open or damaged

- sugar free, dye free, alcohol free - see bottom of cup for lot number and expiration date

Distributed By:

Cardinal Health

Dublin, OH 43017

L55967620320

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Acetaminophen Oral Solution, USP

160 mg/ 5 mL

5 Cups

bag label
bag label

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6738-70ML - Milliliter0904-67382361b563-97fd-46bc-a28c-50ac353e54e812019-05-02

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55154-808855154-8088-5
0904-6738

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
SODIUM BENZOATEOJ245FE5EUIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
SORBITOL506T60A25RIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
METHYLCELLULOSE (15 MPA.S)NPU9M2E6L8IACT
SUCRALOSE96K6UQ3ZD4IACT
XANTHAN GUMTTV12P4NEEIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PROPYLPARABENZ8IX2SC1OHIACT
ACETAMINOPHEN362O9ITL9DACTIB

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
b4dadf84-15b9-4288-85c1-f04b4c8ee69a661886e0-d8df-41e6-ae42-ab6f0144fa762022-12-28WarningsExact identifier
spl set id: 661886e0-d8df-41e6-ae42-ab6f0144fa76

Reported adverse events (FAERS/openFDA)#

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