CHILDRENS IBUPROFEN BUBBLEGUM - ibuprofen suspension/ drops 
CHILDRENS IBUPROFEN GRAPE - ibuprofen suspension/ drops 
CHILDRENS IBUPROFEN BLUE RASPBERRY - ibuprofen suspension/ drops 
CHILDRENS IBUPROFEN FRUIT - ibuprofen suspension/ drops 
Guardian Drug Company

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Guardian Children's Ibuprofen Oral Suspension 

ACTIVE INGREDIENT (in each 5 mL)

Ibuprofen, USP 100 mg (NSAID)*
*nonsteroidal anti-inflammatory drug

PURPOSE

Pain reliever/fever reducer

USE(S)

temporarily:


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 your child:



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

Sore throat warning:
Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by doctor.

DO NOT USE

ASK A DOCTOR BEFORE USE IF

ASK A DOCTOR OR PHARMACIST BEFORE USE IF THE CHILD IS

WHEN USING THIS PRODUCT

STOP USE AND ASK DOCTOR IF

KEEP OUT OF REACH OF CHILDREN

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

DIRECTIONS


Dosing Chart


Weight (lb) Age (yr) Dose (mL)* 
 under 24 under 2 years ask a doctor
 24-35 lbs 2-3 years 5 mL
 36-47 lbs 4-5 years 7.5 mL
 48-59 lbs 6-8 years 10 mL
 60-71 lbs 9-10 years 12.5 mL
 72-95 lbs 11 years 15 mL

*or as directed by a doctor



OTHER INFORMATION

INACTIVE INGREDIENTS

bubblegum flavor: anhydrous citric acid, FD&C red no. 40, flavor, glycerin, polysorbate 80, pregelatinized starch, purified water, sodium benzoate, sucrose, xanthan gum


grape flavor: anhydrous citric acid, D&C red no. 33, FD&C blue no. 1, FD&C red no. 40, flavors, glycerin, polysorbate 80, pregelatinized starch, purified water, sodium benzoate, sucrose, xanthan gum


fruit flavor: anhydrous citric acid, FD&C red no. 40, flavors, glycerin, polysorbate 80, pregelatinized starch, purified water, sodium benzoate, sucrose, xanthan gum


blue raspberry flavor: anhydrous citric acid, FD&C blue no. 1, flavors, glycerin, polysorbate 80, pregelatinized starch, purified water, sodium benzoate, sucrose, xanthan gum

QUESTIONS OR COMMENTS?

call 1-609-860-2600 (Monday - Friday 8 am - 4 pm)

PRINCIPAL DISPLAY PANEL

NDC 53041-572-03

GUARDIAN
For Ages 2 to 11 Years
Children's Ibuprofen
Oral Suspension, USP (NSAID)
100 mg per 5 mL
Pain Reliever/Fever Reducer


Bubble Gum Flavor
4 FL OZ (120 mL)

572


 



PRINCIPAL DISPLAY PANEL

NDC 53041-639-03

GUARDIAN
For Ages 2 to 11 Years
Children's Ibuprofen
Oral Suspension, USP (NSAID)
100 mg per 5 mL
Pain Reliever/Fever Reducer


Grape Flavor
4 FL OZ (120 mL)

639


  

PRINCIPAL DISPLAY PANEL

NDC 53041-632-03

GUARDIAN
For Ages 2 to 11 Years
Children's Ibuprofen
Oral Suspension, USP (NSAID)
100 mg per 5 mL
Pain Reliever/Fever Reducer


Fruit Flavor
4 FL OZ (120 mL)

638

 


PRINCIPAL DISPLAY PANEL

NDC 53041-638-03

GUARDIAN
For Ages 2 to 11 Years
Children's Ibuprofen
Oral Suspension, USP (NSAID)
100 mg per 5 mL
Pain Reliever/Fever Reducer


Blue Raspberry Flavor
4 FL OZ (120 mL)


221



CHILDRENS IBUPROFEN BUBBLEGUM 
ibuprofen suspension/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53041-572
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorPINKScore    
ShapeSize
FlavorBUBBLE GUMImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53041-572-031 in 1 CARTON10/13/2021
1120 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:53041-572-041 in 1 CARTON10/13/2021
2240 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21014910/13/2021
CHILDRENS IBUPROFEN GRAPE 
ibuprofen suspension/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53041-639
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorPURPLEScore    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53041-639-031 in 1 CARTON10/13/2021
1120 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:53041-639-041 in 1 CARTON10/13/2021
2240 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21014910/13/2021
CHILDRENS IBUPROFEN BLUE RASPBERRY 
ibuprofen suspension/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53041-638
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorBLUEScore    
ShapeSize
FlavorRASPBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53041-638-031 in 1 CARTON10/13/2021
1120 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:53041-638-041 in 1 CARTON10/13/2021
2240 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21014910/13/2021
CHILDRENS IBUPROFEN FRUIT 
ibuprofen suspension/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53041-632
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorREDScore    
ShapeSize
FlavorFRUITImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53041-632-031 in 1 CARTON10/13/2021
1120 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:53041-632-041 in 1 CARTON10/13/2021
2240 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21014910/13/2021
Labeler - Guardian Drug Company (119210276)
Establishment
NameAddressID/FEIBusiness Operations
Guardian Drug Company119210276MANUFACTURE(53041-572, 53041-632, 53041-638, 53041-639)

Revised: 10/2021
Document Id: e690a788-b856-44b3-afff-bb950d1eb117
Set id: 9cb92af9-a829-4f54-b8f5-4e5cb4f165b7
Version: 2
Effective Time: 20211013
 
Guardian Drug Company