MedPath

Good Sense Ibuprofen

Perrigo Children’s Ibuprofen Oral Suspension Drug Facts

Approved
Approval ID

1a6b42be-c0c2-48f8-9ba3-22d1f0c0b18d

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Apr 18, 2025

Manufacturers
FDA

L. Perrigo Company

DUNS: 006013346

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Ibuprofen

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0113-0685
Application NumberANDA074937
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ibuprofen
Product Specifications
Route of AdministrationORAL
Effective DateApril 18, 2025
FDA Product Classification

INGREDIENTS (10)

GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
HIGH FRUCTOSE CORN SYRUPInactive
Code: XY6UN3QB6S
Classification: IACT
SORBITOL SOLUTIONInactive
Code: 8KW3E207O2
Classification: IACT
XANTHAN GUMInactive
Code: TTV12P4NEE
Classification: IACT
HYPROMELLOSE, UNSPECIFIEDInactive
Code: 3NXW29V3WO
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BENZOATEInactive
Code: OJ245FE5EU
Classification: IACT
IBUPROFENActive
Quantity: 100 mg in 5 mL
Code: WK2XYI10QM
Classification: ACTIB
ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSL
Classification: IACT

Drug Labeling Information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOINC: 51945-4Updated: 4/18/2025

INDICATIONS & USAGE SECTION

LOINC: 34067-9Updated: 3/6/2013

OTC - QUESTIONS SECTION

LOINC: 53413-1Updated: 6/3/2009

OTC - ACTIVE INGREDIENT SECTION

LOINC: 55106-9Updated: 12/9/2017

OTC - PURPOSE SECTION

LOINC: 55105-1Updated: 12/8/2015

WARNINGS SECTION

LOINC: 34071-1Updated: 12/9/2017

INACTIVE INGREDIENT SECTION

LOINC: 51727-6Updated: 6/3/2009

DOSAGE & ADMINISTRATION SECTION

LOINC: 34068-7Updated: 12/9/2017

STORAGE AND HANDLING SECTION

LOINC: 44425-7Updated: 12/9/2017

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Good Sense Ibuprofen - FDA Drug Approval Details