Ob Towelette
FDA Label NDC 50730-5102

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by H And P Industries, Inc. Dba Triad Group for the product Ob Towelette (NDC 50730-5102). 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, purpose, use, warnings, do not, ask a doctor in case of, otc - ask doctor/pharmacist, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzalkonium chloride .4%

Purpose

Antiseptic

Use

Antiseptic to help prevent the risk of infection

Warnings

For external use only.


Do Not

  • use in the eyes
  • use as a first aid antiseptic longer than one week
  • apply over large areas of the body

Ask A Doctor In Case Of

  • deep or puncture wounds
  • animal bites
  • serious burns

Otc - Ask Doctor/Pharmacist


Otc - When Using


Stop Use And Ask A Doctor

If condition persists or gets worse

Otc - Pregnancy Or Breast Feeding


Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • clean the affected area
  • apply a small amount of this product to the area 1-3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other


Inactive Ingredients

Fragrance, o-phenylphenol, sodium bicarbonate, water

Otc - Questions


Carton Information

TRIADCat. No. 10-5102NDC 50730-5102-0Obstetrical Antiseptic TowelettesHelps prevent the risk of skin infectionsFor Professional and Hospital Use Only100 towelettes

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