Quick answers
- What is Phellodendron amurense bark and purslane used for?
- The Drug Facts label of Wart Remover Cream (Guangzhou Chuanglian Zhida Trading Co., Ltd) lists these uses: Suitable for subhealthy individuals experiencing localized discomfort caused by plantar warts, filiform warts, digitate warts, common warts,flat warts, seborrheic keratosis (senile warts), corns, etc.
- Do I need a prescription for Phellodendron amurense bark and purslane?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Phellodendron amurense bark and purslane been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Wart Remover Cream · Guangzhou Chuanglian Zhida Trading Co., Ltd
Phellodendron amurense bark 0.2% · Purslane 0.3%, cream (topical)
Active ingredient
Purslane(0.3%) Phellodendron Bark(0.2%)
Purpose
Wart Remover
Uses
Suitable for subhealthy individuals experiencing localized discomfort caused by plantar warts, filiform warts, digitate warts, common warts,flat warts, seborrheic keratosis (senile warts), corns, etc.
Warnings
For external use only. Avoid contact with eyes and mouth.
Keep out of reach of children
to prevent accidental ingestion. Discontinue use and consult a physician if allergic reactions or discomfort occur.
Directions
Clean the affected area, apply an appropriate amount to the discomforted area until absorbed.Recommended usage: 2-3 times daily.
Inactive ingredients
ISATIS LEAF DICTAMNUS ROOT BARK EQUISETUM HYEMALE SAFFLOWER PEACH SEED RED PEONY ROOT PEG-400 GLYCERIN WHITE PETROLEUM JELLY STEARYL ALCOHOL CARBOMER BORNEOL CAMPHOR PURIFIED WATER
— FDA label of Wart Remover Cream, Guangzhou Chuanglian Zhida Trading Co., Ltd, effective June 25, 2026. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Phellodendron amurense bark 0.2% · Purslane 0.3% · cream (topical) · 2 products
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Guangzhou Chuanglian Zhida Trading Co., Ltd1 product
- Dongkou County Hecheng Network Technology Co., Ltd.1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youA pharmacist can answer questions about this label
- Latest FDA drug recallsPrescription and over-the-counter, newest first
- All over-the-counter medicinesSearch by ingredient, brand or Spanish name
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.