CALMATROL- diphenhydramine capsule 
Goldman Pharmaceutical Group Inc

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Calmatrol®

Drug Facts

Active ingredient (in each capsule)Purpose
Diphenhydramine HCl 25 mgAntihistamine

Uses

Warnings

Do not use with any other product containing diphenhydramine

Directions

Other information

Inactive Ingredients

D&C red #28, FD&C blue #1, FD&C red #40, gelatin, lactose and starch

Questions or Comments

800.981.7642
petsotc.com

Distributed by
Goldman Pharmaceutical Group Inc.
Holbrook, NY 11741

Tamper-evident : Do not use if carton is open or blister unit is broken or torn

MADE IN AMERICA

PRINCIPAL DISPLAY PANEL - 25 mg Capsule Blister Pack Carton

pet
otc™
over the counter

Calmatrol®
(Diphenhydramine HCl, 25mg) Antihistamine

HELPS TO
RELIEVE:
Anxiety
Hyperactivity
Destructive behavior

12 - 25 lbs

10 CAPSULES

MADE IN THE USA

Highly recommended by
veterinarians

NDC 72087-021-10

PRINCIPAL DISPLAY PANEL - 25 mg Capsule Blister Pack Carton
CALMATROL 
diphenhydramine capsule
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:72087-021(NDC:0904-2035)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
STARCH, CORN (UNII: O8232NY3SJ)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
Product Characteristics
ColorPINK (pink) Scoreno score
ShapeCAPSULESize14mm
FlavorImprint Code 44;107
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72087-021-1010 in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER03/01/2019
Labeler - Goldman Pharmaceutical Group Inc (080389804)
Registrant - Goldman Pharmaceutical Group, Inc. (080389804)
Establishment
NameAddressID/FEIBusiness Operations
Goldman Pharmaceutical Group, Inc.080389804REPACK

Revised: 2/2019
Document Id: 81751193-2172-4a51-8910-42e91c14638f
Set id: c10c0c55-b214-4e73-a3c5-ba1a30e4955f
Version: 1
Effective Time: 20190219
 
Goldman Pharmaceutical Group Inc