Hemorrhoidal
FDA Label NDC 63941-201

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Valu Merchandisers, Co. for the product Hemorrhoidal (NDC 63941-201). 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 uses, warnings, ask a doctor before use if you have, 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,, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Uses

  • helps relieve the local itching and discomfort associated with hemorrhoids
  • temporarily shrinks hemorrhoidal tissue and relieves burning
  • temporarily provides a coating for relief of anorectal discomforts
  • temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

Other Information

Other information

Store at 20 o to 25 oC (68 o to 77 oF)

Inactive Ingredients

beeswax, benzoic acid, BHT, cocoa butter, cod liver oil, glycerin, lanolin, methylparaben, paraffin, propylparaben, purified water, squalane, thyme oil, tocopherol acetate

Active Ingredients

Mineral oil 14%

Petrolatum 71.9%

Phenylephrine HCL 0.25%

Purpose

Protectant

Protectant

Vasoconstrictor


Package Label

Best Choice Hemorrhoidal Ointment

Image Of Carton Label (Bchemoroint.carton)

Image Of Carton Label (Bchemoroint.carton)

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