Conrx Allergy
FDA Label NDC 68737-230

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Eagle Distributors,inc. for the product Conrx Allergy (NDC 68737-230). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, active ingredient (in each caplet), purpose, uses, otc - do not use, ask a doctor before use if you have, otc - ask doctor/pharmacist, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient (In Each Caplet)

Diphenydramine HCl 25 mg

Purpose

Antihistamine

Uses

  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    • runny nose
    • sneezing
    • itchy, watery eyes
    • itching of the nose or throat
    • temporarily relieves these symptoms due to the common cold:
      • runny nose
      • sneezing

Otc - Do Not Use

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

Otc - Ask Doctor/Pharmacist

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

Otc - Pregnancy Or Breast Feeding

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

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Overdose Warning

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

Directions

  • take every 4 to 6 hours
  • do not take more than 6 times in 24 hours

    • 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

  • store between 20-25°C (68-77°F). Avoid high humidity. Protect from light
  • do not use if pouch is torn or open
  • see side panel for lot number and expiration date

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)

Principal Display Panel (50 Pouch Box)

* Please review the disclaimer below.