Universal Witch Hazel Solution
FDA Label NDC 52000-414
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Universal Distribution Center Llc for the product Universal Witch Hazel (NDC 52000-414). 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 drug facts, active ingredients:, purpose, usage:, warning:, otc - keep out of reach of children, direction:, ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients:
All natural distilled witch hazel 100%
(contains natural grain alcohol 14%)
Purpose
Astringent
Usage:
The soft toner is specifically developed to meet ultimate needs of purifying and conditioning for an array of skin types. It is a calm and non-drying formula which removes remaining traces of soap. It removes make-up or excess oils making your skin feeling soft, healthful, and smooth. It also smoothens the skin after shaving. Use as often as necessary. Apply directly from the bottle or dampen a cotton pad and smoothly wipe it off.
Warning:
For external use only. Avoid contact with eyes. If contact occurs, flush thoroughly with water.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Direction:
• remove protective inner seal
• moisten cotton ball or cleansing pad and gently wipe skin
• apply as often as necessary
Ingredients:
Water, Hamamelis Virginiana (Witch Hazel) Leaf Water, Alcohol (14% by Volume), Benzyl Alcohol, Methylchloroisothiazolinone, methylisothiazolinone.
Packaging
Witchhazel-414 (7577101432)
* Please review the disclaimer below.
