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Relief Towelette

Medically reviewed on December 4, 2017

Dosage form: solution
Ingredients: witch hazel .5mL
Labeler: H and P Industries, Inc. dba Triad Group
NDC Code: 50730-5400

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.

Drug Facts

Active ingredient

Witch Hazel 50%



UseFor temporary relief of local discomfort, burning, and irritation associated with hemorrhoids.

Warnings For external use only.
Avoid contact with eyes.

Do notput this product into the rectum using fingers or any mechanical device or applicator.

Stop use and ask a doctor
  • if condition worsens or does not improve within 7 days
  • in case of bleeding
  • before exceeding the recommended dosage.

Keep out of reach of children

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

  • When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly.
  • Gently dry by patting or blotting with toilet tissue or soft cloth before each application of this product. Gently apply to the affected area by patting and then discard. Apply to the affected area up to 6 times daily or after each bowel movement.
  • Children under 12 years of age: consult a doctor.

Other information Store at room temperature 15° -30° C (59° - 86° F)

Inactive Ingredientscitric acid, diazolidinyl urea, glycerin, methylparaben, propylene glycol, propylparaben, sodium citrate, water

Package InformationCat. No. 10-5400
NDC 50730-5400-0

Medicated hemorrhoidal towelettes
Comfort, soothe, cool - pH balanced

Triad Group, Inc.
700 West North Shore Drive
Hartland, WI 53029 USA

Made in USA

100 Towelettes

witch hazel solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50730-5400
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
witch hazel (witch hazel) witch hazel.5 mL
Inactive Ingredients
Ingredient NameStrength
citric acid monohydrate 
propylene glycol 
sodium citrate 
#Item CodePackage Description
1NDC:50730-5400-0100 POUCH (POUCH) in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34610/17/1994
Labeler - H and P Industries, Inc. dba Triad Group (050259597)
Registrant - H and P Industries, Inc. dba Triad Group (050259597)
H and P Industries, Inc. dba Triad Group050259597manufacture

H and P Industries, Inc. dba Triad Group

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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