Label: MEDICATED PAD- witch hazel solution
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Contains inactivated NDC Code(s)
NDC Code(s): 50730-7549-1 - Packager: H and P Industries, Inc. dba Triad Group
- Category: HUMAN OTC DRUG LABEL
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 Label Information
Updated December 8, 2009
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
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DIRECTIONS
- 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
- OTHER USES
- INACTIVE INGREDIENTS
- QUESTIONS
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LABEL INFORMATION
NDC 50730-7549-1
Compare to the active ingredient in TUCKS®.
Hemorrhoidal
Pads
- Pre-moistened Hemorrhoidal/Vaginal Pads with Witch Hazel
- Provides Temporary Relief of Burning, Itching and Local Discomfort Associated with Hemorrhoids
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. -
INGREDIENTS AND APPEARANCE
MEDICATED PAD
witch hazel solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50730-7549 Route of Administration RECTAL, TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength witch hazel (UNII: 101I4J0U34) (witch hazel - UNII:101I4J0U34) witch hazel .5 mL in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:50730-7549-1 100 in 1 JAR 1 2.5 mL in 1 APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 02/01/2007 Labeler - H and P Industries, Inc. dba Triad Group (050259597)