IBUPROFEN- ibuprofen capsule, liquid filled 
Bionpharma Inc.

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Drug Facts

Active ingredient (in each capsule)

Solubilized ibuprofen equal to 200 mg ibuprofen (NSAID)*
(present as the free acid and potassium salt)
*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/Fever reducer

Uses

Warnings

Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

If an allergic reaction occurs, stop use and seek medical help right away.

Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you

Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be be fatal. The risk is higher if you use more than directed or for longer than directed.

Do not use

Ask a doctor before use if

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

If pregnant or breast- feeding,

ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

FD&C Blue #1, gelatin, pharmaceutical ink, polyethylene glycol, potassium hydroxide, purified water, sorbitan and sorbitol

Questions or comments?

call toll free 1-888-235-2466

All trademarks are property of their respective owners. This product is not affiliated with the owners of Advil ® LIQUI-GELS ®

DO NOT USE IF TAMPER-EVIDENT SEAL UNDER BOTTLE CAP IMPRINTED WITH “ SEALED for YOUR PROTECTION” IS BROKEN OR MISSING.

Manufactured for:

Bionpharma Inc.

600 Alexander Road

Princeton, NJ 08540

Rev# 12/20

L0000393

360's Bottle Label

100 Capsules

IBUPROFEN 
ibuprofen capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69452-212
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GELATIN (UNII: 2G86QN327L)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
WATER (UNII: 059QF0KO0R)  
SORBITAN (UNII: 6O92ICV9RU)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
ColorblueScoreno score
ShapeCAPSULESize20mm
FlavorImprint Code IB200
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69452-212-1120 in 1 BOTTLE; Type 1: Convenience Kit of Co-Package11/01/201811/01/2018
2NDC:69452-212-1540 in 1 BOTTLE; Type 1: Convenience Kit of Co-Package11/01/201811/01/2018
3NDC:69452-212-7880 in 1 BOTTLE; Type 1: Convenience Kit of Co-Package11/01/201811/01/2018
4NDC:69452-212-20100 in 1 BOTTLE; Type 1: Convenience Kit of Co-Package11/01/201811/01/2018
5NDC:69452-212-79160 in 1 BOTTLE; Type 1: Convenience Kit of Co-Package11/01/201811/01/2018
6NDC:69452-212-83300 in 1 BOTTLE; Type 0: Not a Combination Product11/01/201811/01/2018
7NDC:69452-212-90360 in 1 BOTTLE; Type 0: Not a Combination Product02/04/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07868211/01/2018
Labeler - Bionpharma Inc. (079637826)
Registrant - Bionpharma Inc. (079637826)
Establishment
NameAddressID/FEIBusiness Operations
Patheon Softgels Inc.002193829manufacture(69452-212)

Revised: 2/2021
Document Id: ba8b0cb0-fdef-da33-e053-2a95a90a65fd
Set id: 4bc6e8f2-ba95-4352-80ed-b44608fc4936
Version: 2
Effective Time: 20210204
 
Bionpharma Inc.