IBUPROFEN AND DIPHENHYDRAMINE CITRATE - ibuprofen and diphenhydramine citrate tablet, coated 
Aurohealth LLC

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Diphenhydramine Citrate and Ibuprofen Tablets USP 38 mg/200 mg

Drug Facts

Active ingredients
(in each caplet)

Diphenhydramine citrate USP 38 mg
Ibuprofen USP 200 mg (NSAID)*
*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 (1-800-222-1222) right away.

Directions

Other information


Inactive ingredients

carnauba wax, colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C blue # 2, glyceryl dibehenate, hypromellose, lactose monohydrate, microcrystalline cellulose, palmitic acid, polydextrose, polyethylene glycol, pregelatinized starch (maize), sodium lauryl sulfate, sodium starch glycolate, stearic acid, and titanium dioxide.

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 No.: TS/DRUGS/16/2014

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg/38 mg (20 Coated Caplets) Bottle Label

AUROHEALTH
NDC 58602-867-73
Ibuprofen and
Diphenhydramine Citrate
Tablets
200 mg/38 mg
Pain Reliever (NSAID)/Nighttime Sleep-Aid
20
Coated Caplets*                  *Capsule-Shaped Tablets



PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg/38 mg (20 Coated Caplets) Bottle Label



PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg/38 mg (20 Coated Caplets) Bottle Carton Label

AUROHEALTH
NDC 58602-867-73
Compare to the active
ingredients in Advil® PM
Ibuprofen and
Diphenhydramine Citrate
Tablets
200 mg/38 mg
Pain Reliever (NSAID)/
Nighttime Sleep-Aid
20
Coated Caplets*
*Capsule-Shaped Tablets            200 
                                                      Actual size   

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg/38 mg (20 Coated Caplets) Bottle Carton Label

IBUPROFEN AND DIPHENHYDRAMINE CITRATE 
ibuprofen and diphenhydramine citrate tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58602-867
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
DIPHENHYDRAMINE CITRATE (UNII: 4OD433S209) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE CITRATE38 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX (UNII: R12CBM0EIZ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STARCH, CORN (UNII: O8232NY3SJ)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)  
HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)  
HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)  
MICROCRYSTALLINE CELLULOSE 102 (UNII: PNR0YF693Y)  
PALMITIC ACID (UNII: 2V16EO95H1)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorBLUEScoreno score
ShapeCAPSULESize15mm
FlavorImprint Code DI;200
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58602-867-731 in 1 CARTON05/31/2022
120 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:58602-867-091 in 1 CARTON05/31/2022
230 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:58602-867-121 in 1 CARTON05/31/2022
340 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:58602-867-141 in 1 CARTON05/31/2022
450 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:58602-867-181 in 1 CARTON05/31/2022
580 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:58602-867-211 in 1 CARTON05/31/2022
6100 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:58602-867-231 in 1 CARTON05/31/2022
7120 in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:58602-867-27140 in 1 BOTTLE; Type 0: Not a Combination Product05/31/2022
9NDC:58602-867-32180 in 1 BOTTLE; Type 0: Not a Combination Product05/31/2022
10NDC:58602-867-34200 in 1 BOTTLE; Type 0: Not a Combination Product05/31/2022
11NDC:58602-867-701 in 1 CARTON05/31/2022
1140 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
12NDC:58602-867-781 in 1 CARTON05/31/2022
1250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
13NDC:58602-867-721 in 1 CARTON05/31/2022
1380 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
14NDC:58602-867-97120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/31/2022
15NDC:58602-867-46140 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/31/2022
16NDC:58602-867-92180 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/31/2022
17NDC:58602-867-80200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21620405/31/2022
Labeler - Aurohealth LLC (078728447)
Establishment
NameAddressID/FEIBusiness Operations
APL HEALTHCARE LIMITED650844777ANALYSIS(58602-867) , MANUFACTURE(58602-867)

Revised: 6/2022
Document Id: 21c1f5c5-19fa-4a59-bad3-ea85fd37471b
Set id: 21c1f5c5-19fa-4a59-bad3-ea85fd37471b
Version: 1
Effective Time: 20220603
 
Aurohealth LLC