DIPHENHYDRAMINE HCL AND IBUPROFEN - diphenhydramine hcl and ibuprofen capsule, liquid filled 
Aurohealth LLC

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Diphenhydramine HCL and Ibuprofen Capsules USP 25 mg/200 mg

Drug Facts

Active ingredients
(in each capsule)

Diphenhydramine hydrochloride USP 25 mg
Solubilized ibuprofen equal to 200 mg ibuprofen USP (NSAID)*
(present as the free acid and potassium salt)
*nonsteroidal anti-inflammatory drug

Purposes

Nighttime sleep-aid
Pain reliever

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 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 at 20 weeks or later in 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. [1-800-222-1222]

Directions


Other information


Inactive ingredients

D&C Red No.33, gelatin, Neelicert FD&C Blue No.1, polyethylene glycol, potassium hydroxide, povidone, purified water, sorbitol sorbitan solution.

Questions or comments?

Call 1-855-274-4122 (Monday – Friday 8:30 AM to 5:00 PM EST)

Distributed by:
AUROHEALTH LLC
279 Princeton-Hightstown Road
East Windsor, NJ 08520

Made in India

Code: TS/DRUGS/16/2014

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Label

AUROHEALTH
NDC 58602-887-73
Diphenhydramine
HCl and Ibuprofen
Capsules USP
25 mg/200 mg
Nighttime Sleep-Aid/
Pain Reliever (NSAID)
20 Liquid Filled Capsules
READ AND KEEP CARTON FOR COMPLETE
WARNINGS AND INFORMATION

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Label



PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Carton Label

AUROHEALTH                    

NDC 58602-887-73

Diphenhydramine HCl
and Ibuprofen Capsules USP
25 mg/200 mg

Nighttime Sleep-Aid/Pain Reliever (NSAID)

20 Liquid Filled Capsules

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 25 mg/200 mg (20 Liquid-Filled Capsules) Bottle Carton Label

DIPHENHYDRAMINE HCL AND IBUPROFEN 
diphenhydramine hcl and ibuprofen capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58602-887
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
1,4-SORBITAN (UNII: AV0YTZ4E6J)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
MANNITOL (UNII: 3OWL53L36A)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
POVIDONE K30 (UNII: U725QWY32X)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
ColorBLUEScoreno score
ShapeOVALSize15mm
FlavorImprint Code DHI25
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58602-887-731 in 1 CARTON08/10/2022
120 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:58602-887-101 in 1 CARTON08/10/2022
232 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:58602-887-121 in 1 CARTON08/10/2022
340 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:58602-887-181 in 1 CARTON08/10/2022
480 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:58602-887-23120 in 1 BOTTLE; Type 0: Not a Combination Product08/10/2022
6NDC:58602-887-30160 in 1 BOTTLE; Type 0: Not a Combination Product08/10/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21067608/10/2022
Labeler - Aurohealth LLC (078728447)
Establishment
NameAddressID/FEIBusiness Operations
APL HEALTHCARE LIMITED650844777ANALYSIS(58602-887) , MANUFACTURE(58602-887)
Establishment
NameAddressID/FEIBusiness Operations
Aurobindo Pharma Limited650381903ANALYSIS(58602-887) , MANUFACTURE(58602-887)

Revised: 8/2022
Document Id: 2c7c5349-06c9-401a-88e9-8f91ddb7f91a
Set id: 2c7c5349-06c9-401a-88e9-8f91ddb7f91a
Version: 1
Effective Time: 20220819
 
Aurohealth LLC