MEDICATED PAD - witch hazel solution 
H and P Industries, Inc. dba Triad Group

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.

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DRUG FACTS

ACTIVE INGREDIENT

Witch Hazel 50% v/v

PURPOSE

Hemorrhoidal Astringent

USES

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

WARNINGS

For external use only. Avoid contact with eyes.

Consult a doctor

  • if condition worsens or does not improve within 7 days
  • in case of bleeding
  • before exceeding the recommended dosage

Do not

put this product into rectum using fingers or any mechanical device or applicator






Keep out of reach of children

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

DIRECTIONS

OTHER INFORMATION

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

OTHER USES

For vaginal care - Cleanse the area by gently wiping, patting or blotting with pad and discard. Repeat as needed.

INACTIVE INGREDIENTS

citric acid, diazolidinyl urea, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate


LABEL INFORMATION

NDC 50730-7549-1
Compare to the active ingredient in TUCKS®.

Hemorrhoidal
Pads


100 MEDICATED PADS

SAFEWAY

For your protection, jar is sealed. Remove lid. If seal is broken or missing, do not use.

DISTRIBUTED BY SAFEWAY INC.
PO BOX 99, PLEASANTON, CA 94566-0009

This product is not manufactured or distributed by Parke-Davis, owner of the registered trademark TUCKS® Medicated Pads.

label

MEDICATED PAD 
witch hazel solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50730-7549
Route of AdministrationRECTAL, TOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
witch hazel (UNII: 101I4J0U34) (witch hazel - UNII:101I4J0U34) witch hazel.5 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
citric acid monohydrate (UNII: 2968PHW8QP)  
diazolidinylurea (UNII: H5RIZ3MPW4)  
glycerin (UNII: PDC6A3C0OX)  
methylparaben (UNII: A2I8C7HI9T)  
propylene glycol (UNII: 6DC9Q167V3)  
propylparaben (UNII: Z8IX2SC1OH)  
sodium citrate (UNII: 1Q73Q2JULR)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50730-7549-1100 in 1 JAR
12.5 mL in 1 APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34602/01/2007
Labeler - H and P Industries, Inc. dba Triad Group (050259597)

Revised: 12/2009
Document Id: b0f0c2af-ef39-47ea-b3b4-af08a5c095e8
Set id: e3c255d9-9378-4768-8423-472cefd7782d
Version: 1
Effective Time: 20091208
 
H and P Industries, Inc. dba Triad Group