CONRX ALLERGY- diphenhydramine hydrochloride tablet 
Eagle Distributors,Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ConRx™ Allergy

Drug Facts

Active ingredient (in each caplet)

Diphenydramine HCl 25 mg

Purpose

Antihistamine

Uses

Warnings

Do not use with any other product containing diphenhydramine, even one used on skin.

Ask a doctor before use if you have

  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

When using this product

  • marked drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • excitabiity may occur, especially in children

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Overdose warning

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

Directions

adults and children 12 years and over 1 to 2 caplets

children 6 to under 12 years 1 caplet,

children under 6 years consult a doctor

Other information

Inactive ingredients

croscarmellose sodium, D&C Red #27, hydroxypropylmethyl cellulose, lactose, magnesium stearate, microcrystalline cellulose, polythylene glycol, silicon dioxide, titanium dioxide. May contain polysorbate.

Questions or comments?

1-800-570-8650

PRINCIPAL DISPLAY PANEL - 50 Pouch Box

Compare to the Active Ingredients in

Benadryl®*

ConRx™ Allergy

■ Watery Eyes ■ Sneezing ■ Runny Nose

Diphenhydramine Hci | Antihistamine

TO OPEN
PUSH IN TAB AND PULL OUT

Compare to the Active Ingredients in
Benadryl®*

50 Pouches of 2 Caplets Each

Principal Display Panel - 50 Pouch Box
CONRX ALLERGY 
diphenhydramine hydrochloride tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:68737-230
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Diphenhydramine Hydrochloride (UNII: TC2D6JAD40) (Diphenhydramine - UNII:8GTS82S83M) Diphenhydramine Hydrochloride 25 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C RED NO. 27 (UNII: 2LRS185U6K)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
Product Characteristics
Color RED Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code CRX
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68737-230-14 50 in 1 BOX
1 2 in 1 POUCH
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part341 02/15/2013
Labeler - Eagle Distributors,Inc. (929837425)

Revised: 2/2013
Document Id: ba486804-de1f-4762-959a-42aa87259b98
Set id: df991bb2-88f8-41d1-b58a-c6c7993c036b
Version: 1
Effective Time: 20130211
 
Eagle Distributors,Inc.