Active Ingredient
Witch Hazel 50% v/v
The following Structured Product Label (SPL) was submitted to the FDA by H And P Industries, Inc. Dba Triad Group for the product Medicated Pad (NDC 50730-7549). 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, uses, warnings, consult a doctor, do not, otc - ask doctor/pharmacist, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Witch Hazel 50% v/v
Hemorrhoidal Astringent
For external use only. Avoid contact with eyes.
If swallowed, get medical help or contact a Poison Control Center right away.
Store at room temperature: 15°- 30° C (59° - 86° F)
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.
* Please review the disclaimer below.