Witch Hazel
Witch Hazel is an FDA drug label for the active ingredient WITCH HAZEL manufactured by Pharma Nobis, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231222.
Generic: WITCH HAZEL
Manufacturer: Pharma Nobis, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 82645-903
Application: M017
Effective: 20231222
Active Ingredients: Active Ingredient Witch Hazel
Indications & Usage
Indications For relief of minor skin Irritations due to minor cuts minor scraps insect bites
Dosage & Administration
Directions Apply liberally to the afflicted area as often as necessary
Contraindications
Not available.
Warnings
Warnings For external use only avoid contact with eyes If contact occurs rinse thoroughly with water.
Adverse Reactions
Not available.
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