Pharbedryl
FDA Label NDC 67046-006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Contract Pharmacy Services-pa for the product Pharbedryl (NDC 67046-006). 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 active ingredient(in each banded capsule), purpose, uses:, do not use, ask a doctor before use if you have, ask doctor or pharmacist before use if you are, when using this product, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient(In Each Banded Capsule)

Diphenhydramine HCl 50 mg

Do Not Use

  • With any other product containing diphenhydramine, even one used on skin.

Ask A Doctor Before Use If You Have

  • Trouble urinating due to enlarged prostate gland
  • A breathing problem such as emphysema or chronic bronchitis
  • Glaucoma

When Using This Product

  • Avoid alcoholic drinks
  • Marked drowsiness may occur.
  • Excitability may occur, especially in children
  • Alcohol, sedatives and tranquilizers may increase drowsiness
  • Be careful when driving a motor vehicle or operating machinery

Directions:

  • Take every 4-6 hours
  • Do not take more than 6 doses in 24 hours.
  • Adults and children 12 years or over
    1 capsule                                     
    Children under 12 years
    ask a doctor

Other Information:

  • Tamper Evident: Do not use if safety seal under cap is broken or missing
  • Store at room temperature 15°-30°C (59°-86°F)
  • Protect from moisture
  • Use by expiration date on package

Questions? Adverse Drug Event Call:

(866) 562-2756

* Please review the disclaimer below.