Active Ingredient
Witch Hazel 50%
The following Structured Product Label (SPL) was submitted to the FDA by H And P Industries, Inc. Dba Triad Group for the product Relief (NDC 50730-7502). 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, stop use and ask 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%
Astringent
For external use only.
If swallowed, get medical help or contact a Poison Control Center right away.
* Please review the disclaimer below.